Deck 10: Patterns of Inheritance

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Question
When two alleles of the same gene are identical, the individual carrying those alleles is said to be ____.

A) dominant
B) heterozygous
C) recessive
D) genotypical
E) homozygous
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Question
An allele is ____ if its effect masks that of a ____ allele paired with it.

A) recessive; codominant
B) codominant; recessive
C) recessive; dominant
D) dominant; recessive
E) incompletely recessive; dominant
Question
Observable traits are known in genetics as ____.

A) phenotypes
B) genotypes
C) homozygous
D) heterozygous
E) homozygous genotypes
Question
In cats, short hair ( L ) is dominant to long hair ( l ). If a short-haired cat of unknown genotype is crossed with a long-haired animal, and they produce one long-haired kitten and one short-haired kitten, this would indicate that ____.

A) the short-haired cat was true-breeding
B) the short-haired cat was not true-breeding
C) the long-haired cat was not true-breeding
D) the long-haired cat was heterozygous
E) neither parent was true-breeding
Question
In a person with cystic fibrosis, the CFTR mutation causes the protein to be ____.

A) embedded in the plasma membrane
B) destroyed in the endoplasmic reticulum
C) shuttled to the nuclear membrane instead of the plasma membrane
D) shuttled to the plasma membrane instead of the nuclear membrane
E) expelled from the cell by exocytosis before it can do its job
Question
Various forms of the same gene are called ____.

A) genotypes
B) alleles
C) somatic
D) recessive
E) phenotypes
Question
Red coat is dominant in horses and white coat is recessive. In a cross between a homozygous dominant red-coated horse and a white-coated horse, what genotype(s) would be observed in the offspring?

A) all homozygous recessive
B) all homozygous dominant
C) half homozygous dominant and half homozygous recessive
D) all heterozygous
E) half heterozygous and half homozygous dominant
Question
____ raises miscarriage risks by 2-10 percent and is rarely performed.

A) Conventional ultrasound
B) Fetoscopy
C) 4D ultrasound
D) Amniocentesis
E) CVS
Question
The mutated gene that causes cystic fibrosis is ____.

A) CFTR
B) CRFT
C) CTFR
D) CRTF
E) CFRT
Question
When Gregor Mendel first started his genetics experiments, he ____.

A) knew about the existence of genes
B) knew that some plants "breed true"
C) knew that genes were responsible for observable traits
D) allowed the pea plants to self-fertilize
E) expected all true breeding crosses to produce offspring with intermediate phenotypes
Question
When two alleles of the same gene are different, the individual carrying those alleles is said to be ____.

A) recessive
B) heterozygous
C) phenotypic
D) somatic
E) homozygous
Question
The most common type of mutation that causes cystic fibrosis is a(n) ____.

A) deletion
B) insertion
C) base-pair substitution
D) gene duplication
E) transformation
Question
The failure of which organ affected by a defective CFTR protein is likely to cause death in cystic fibrosis patients?

A) lungs
B) intestines
C) heart
D) liver
E) reproductive system
Question
If R is dominant to r , the offspring of the cross of RR with rr will ____.

A) have a unique phenotype
B) have the same phenotype as the RR parents
C) have the same phenotype as the rr parents
D) have the same genotype as the RR parents
E) have the same genotype as the rr parents
Question
An individual's ____ determines its observable ____.

A) phenotype; genotype
B) genotype; phenotype
C) gene location; allele
D) heterozygote; homozygote
E) homozygote; heterozygote
Question
If tall ( D ) is dominant to dwarf ( d ), and two homozygous varieties DD and dd are crossed, the progeny produced will be____.

A) all intermediate forms
B) all tall
C) all dwarf
D) 1/2 tall and 1/2 dwarf
E) 3/4 tall and 1/4 dwarf
Question
____ is the most fatal genetic disorder in the United States.

A) Cystic fibrosis
B) Huntington's disease
C) Sickle-cell anemia
D) Anhidrotic dysplasia
E) Color blindness
Question
In the lungs of cystic fibrosis patients, ____.

A) chloride ions are stuck inside epithelial cells
B) water is excessively abundant on epithelial surfaces
C) epithelial surfaces are coated with slippery mucus
D) excess water and chloride ions are pumped out of epithelial cells
E) chloride ions are not transported out of epithelial cells, and epithelial surfaces are dry
Question
The main problem for those with cystic fibrosis involves ____.

A) mucus sticking to dry surfaces
B) jerky muscle contractions
C) constant thirst
D) salt accumulations between tissues
E) low pH in tissues preventing proper enzymatic activity
Question
A(n) ____ is an offspring of a cross between two individuals that breed true for different forms of a given trait.

A) homozygote
B) recessive
C) hybrid
D) phenotype
E) genotype
Question
The mutation that causes the lighter skin color of all people of European descent was the result of a ____ in the gene for a melanin transport protein.

A) base-pair substitution
B) insertion
C) deletion
D) whole chromosome duplication
E) multiple gene mutations involving several mechanisms
Question
Genetic recombination as a result of crossing over occurs more readily between genes that are ____.

A) on the sex chromosomes
B) near the centromere
C) located close together on the same chromosome
D) located far apart on the same chromosome
E) located on different chromosomes
Question
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, how many plants would have white flowers and short stems?</strong> A) 1 B) 3 C) 5 D) 9 E) 16 <div style=padding-top: 35px> Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, how many plants would have white flowers and short stems?

A) 1
B) 3
C) 5
D) 9
E) 16
Question
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( A aBb   ´   AaBb ). In the figure above, how many plants would have purple flowers and tall stems?</strong> A) 1 B) 3 C) 5 D) 9 E) 16 <div style=padding-top: 35px> Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( A aBb   ´   AaBb ).
In the figure above, how many plants would have purple flowers and tall stems?

A) 1
B) 3
C) 5
D) 9
E) 16
Question
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, what would be the genotype of plant #7?</strong> A) AaBb B) AABb C) AaBB D) AABB E) aaBB <div style=padding-top: 35px> Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, what would be the genotype of plant #7?

A) AaBb
B) AABb
C) AaBB
D) AABB
E) aaBB
Question
For this problem, you may want to create a Punnett Square on a separate piece of paper. Manuel has cystic fibrosis, a recessive disorder, and sickle-cell anemia, which is also a recessive disorder. Manuel's partner, Lucretia, is normal for both conditions. What is the probability that Manuel and Lucretia will have a normal child without either of the conditions Manuel has?

A) 0  percent
B) 25  percent
C) 75  percent
D) 100  percent
E) It is not possible to solve this problem with the information provided.
Question
In cats, short hair L is dominant to long hair l and black hair B is dominant to brown hair b . If you found a black, short-haired cat, you could determine his genotype by crossing it to an animal with a genotype of ____.

A) LLBB
B) llBB
C) llBb
D) llbb
E) LLbb
Question
If two individuals who are heterozygous for two traits that display incomplete dominance (e.g., AaBb) mate and have offspring, how many different phenotypes are possible?

A) 1
B) 3
C) 6
D) 9
E) 16
Question
Cystic fibrosis is a recessive disorder. If a couple, each of whom is heterozygous for the CFTR mutation, have children, what is the probability that they will have a child with cystic fibrosis?

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
Question
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, what would be the genotype of plant #9?</strong> A) Aabb B) aaBb C) AaBB D) AABB E) aaBB <div style=padding-top: 35px> Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, what would be the genotype of plant #9?

A) Aabb
B) aaBb
C) AaBB
D) AABB
E) aaBB
Question
The ease of detecting and treating ____ is a good example of the advantages of genetic screening.

A) PKU
B) Tay-Sachs
C) Marfan syndrome
D) color blindness
E) Down syndrome
Question
The discarded theory of blending inheritance most closely resembles ____.

A) X-linked inheritance
B) dihybridization
C) codominance
D) incomplete dominance
E) complete dominance
Question
If a child has an AB blood type, ____.

A) both parents must have different blood types
B) neither parent can have blood type AB
C) both parents must have blood type AB
D) both parents can be any blood type
E) one parent can have blood type O
Question
In a Punnett square, the letters on top of the square and on the side of the square represent ____.

A) offspring genotypes
B) zygote genotypes
C) parental gametes
D) offspring phenotypes
E) parental phenotypes
Question
For this problem, you may want to create a Punnett Square on a separate piece of paper. Assume brown eyes are dominant to blue eyes and dimples are dominant to no dimples. John has brown eyes, and his mother has blue eyes. John does not have dimples. Zena has blue eyes and also has no dimples. What are the chances if this couple have children, they will produce a child with blue eyes and no dimples?

A) 0
B) ¼
C) ½
D) ¾
E) There is not enough information provided to solve this problem.
Question
In codominance, ____.

A) one allele is dominant to another allele
B) the genotype is determined by the phenotype
C) the heterozygous phenotype is intermediate to the homozygous phenotypes
D) the intermediate phenotype may be the result of enzyme insufficiency
E) two alleles may be equally expressed
Question
Approximately how many gene products are involved in the synthesis of melanin in humans?

A) 10
B) 25
C) 50
D) 100
E) 1000
Question
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, how many plants would have the genotype AaBb ?</strong> A) 1 B) 3 C) 4 D) 6 E) 9 <div style=padding-top: 35px> Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, how many plants would have the genotype AaBb ?

A) 1
B) 3
C) 4
D) 6
E) 9
Question
In a cross of a DDRR individual with a ddrr individual, the genotype of all offspring will ____.

A) DDRR
B) DdRR
C) DdRr
D) ddRR
E) ddRr
Question
If a pure-breeding wired-hair terrier ( WW ) is crossed with a pure-breeding smooth-hair terrier (ww), and a puppy with a wavy hair is produced, the simplest explanation is ____.

A) a mutation has occurred
B) hair texture is an X-linked trait
C) incomplete dominance
D) hair texture is a lethal trait
E) codominance
Question
When genes are located very close together on the same chromosome, ____.

A) gametes usually end up with the same combination of alleles as parental cells
B) gametes usually end up with unique combination of alleles
C) they are inherited separately
D) they often recombine during crossing over
E) offspring will look just like one parent
Question
The switching between asexual and sexual reproduction by water fleas is controlled by ____.

A) epistasis
B) pleiotropy
C) incomplete dominance
D) codominant inheritance
E) environmental effects
Question
In an autosomal dominant disorder such as Huntington's disease, two carrier parents have the probability of passing the gene onto ____ of their children.

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
Question
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is the probability that they will be normal?

A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
Question
In a pedigree chart, a male who demonstrates the trait being studied is represented by a ____.

A) darkened square
B) darkened diamond
C) clear circle
D) clear square
E) darkened circle
Question
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is probability that they will be affected by achondroplasia?

A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
Question
In the Bombay phenotype, a gene in the recessive condition blocks the expression of A and B red blood cell antigens. Thus, all A, B, and AB genotypes are expressed as the O phenotype. This is an example of ____.

A) complete dominance
B) polygeny
C) incomplete dominance
D) codominance
E) pleiotropy
Question
A gene that produces multiple effects is called a(n) ____.

A) codominant gene
B) X-linked gene
C) epistatic gene
D) pleiotropic gene
E) incompletely dominant gene
Question
A pleiotropic gene ____.

A) acts on secondary sexual characteristics
B) influences multiple traits
C) is additive
D) produces lethal effects when homozygous
E) produces epigenetic effects
Question
The probability of producing a normal child by two parents who are carriers for an autosomal recessive disorder is ____.

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
Question
An X-linked carrier is a ____.

A) homozygous dominant female
B) heterozygous female
C) homozygous recessive female
D) homozygous male
E) heterozygous male
Question
Geneticists use ____ to study the genetics of families through generations.

A) Punnett squares
B) pedigrees
C) karyotypes
D) DNA profiles
E) fossil analyses
Question
The ABO blood types have ____ different genotypes.

A) 4
B) 6
C) 8
D) 12
E) 16
Question
An autosomal recessive disorder ____.

A) requires that only one parent be a carrier
B) displays its symptoms in heterozygotes
C) is more frequent in males than females
D) requires that both parents are carriers
E) only affects females
Question
Human eye color is an example of a trait that varies ____.

A) according to the geographical area
B) periodically
C) according to humidity
D) continuously
E) according to seasons
Question
In humans, skin color is controlled by several genes. Thus, skin color is a(n) ____ characteristic.

A) dominant
B) codominant
C) polygenic
D) pleiotropic
E) recessive
Question
In a pedigree chart, a female showing the specific trait being studied is indicated by a ____.

A) clear square
B) darkened square
C) clear circle
D) darkened diamond
E) darkened circle
Question
Six fingers on one hand would be classified as a(n) ____.

A) genetic disorder
B) disease
C) syndrome
D) genetic abnormality
E) illness
Question
In Siamese cats, enzymes that code for dark fur color are only active in cooler temperatures. Thus, the tips of a Siamese cat's ears, feet, and tail are dark but not the warmer regions of its body core. This is an example of ____.

A) p leiotropy
B) environmental effects
C) epistasis
D) incomplete dominance
E) codominance
Question
Males are more commonly affected by X-linked recessive genetic disorders than females because ____.

A) females have two X chromosomes; therefore, they do not inherit recessive alleles
B) males have only one X chromosome; therefore, they express all recessive X-linked traits
C) males have only one X chromosome; therefore, they have multiple alleles for each X-linked gene
D) Y chromosomes cause X-linked gene mutations
E) males are genetically weaker than females
Question
Match between columns
polydactyly
autosomal recessive disorder
polydactyly
X-linked disorder
polydactyly
autosomal dominant disorder
polydactyly
mental impairment and heart defects
polydactyly
Sterility and mental impairment
polydactyly
sterility, abnormal ovaries, and abnormal sexual traits
polydactyly
mild mental impairment
polydactyly
minimal abnormalities
polydactyly
codominance
polydactyly
pleiotropy
polydactyly
epistasis
polydactyly
incomplete dominance
polydactyly
continuous variation
XXX syndrome
autosomal recessive disorder
XXX syndrome
X-linked disorder
XXX syndrome
autosomal dominant disorder
XXX syndrome
mental impairment and heart defects
XXX syndrome
Sterility and mental impairment
XXX syndrome
sterility, abnormal ovaries, and abnormal sexual traits
XXX syndrome
mild mental impairment
XXX syndrome
minimal abnormalities
XXX syndrome
codominance
XXX syndrome
pleiotropy
XXX syndrome
epistasis
XXX syndrome
incomplete dominance
XXX syndrome
continuous variation
Marfan syndrome
autosomal recessive disorder
Marfan syndrome
X-linked disorder
Marfan syndrome
autosomal dominant disorder
Marfan syndrome
mental impairment and heart defects
Marfan syndrome
Sterility and mental impairment
Marfan syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Marfan syndrome
mild mental impairment
Marfan syndrome
minimal abnormalities
Marfan syndrome
codominance
Marfan syndrome
pleiotropy
Marfan syndrome
epistasis
Marfan syndrome
incomplete dominance
Marfan syndrome
continuous variation
fur color in Labrador retrievers
autosomal recessive disorder
fur color in Labrador retrievers
X-linked disorder
fur color in Labrador retrievers
autosomal dominant disorder
fur color in Labrador retrievers
mental impairment and heart defects
fur color in Labrador retrievers
Sterility and mental impairment
fur color in Labrador retrievers
sterility, abnormal ovaries, and abnormal sexual traits
fur color in Labrador retrievers
mild mental impairment
fur color in Labrador retrievers
minimal abnormalities
fur color in Labrador retrievers
codominance
fur color in Labrador retrievers
pleiotropy
fur color in Labrador retrievers
epistasis
fur color in Labrador retrievers
incomplete dominance
fur color in Labrador retrievers
continuous variation
Klinefelter syndrome
autosomal recessive disorder
Klinefelter syndrome
X-linked disorder
Klinefelter syndrome
autosomal dominant disorder
Klinefelter syndrome
mental impairment and heart defects
Klinefelter syndrome
Sterility and mental impairment
Klinefelter syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Klinefelter syndrome
mild mental impairment
Klinefelter syndrome
minimal abnormalities
Klinefelter syndrome
codominance
Klinefelter syndrome
pleiotropy
Klinefelter syndrome
epistasis
Klinefelter syndrome
incomplete dominance
Klinefelter syndrome
continuous variation
height in humans
autosomal recessive disorder
height in humans
X-linked disorder
height in humans
autosomal dominant disorder
height in humans
mental impairment and heart defects
height in humans
Sterility and mental impairment
height in humans
sterility, abnormal ovaries, and abnormal sexual traits
height in humans
mild mental impairment
height in humans
minimal abnormalities
height in humans
codominance
height in humans
pleiotropy
height in humans
epistasis
height in humans
incomplete dominance
height in humans
continuous variation
hemophilia
autosomal recessive disorder
hemophilia
X-linked disorder
hemophilia
autosomal dominant disorder
hemophilia
mental impairment and heart defects
hemophilia
Sterility and mental impairment
hemophilia
sterility, abnormal ovaries, and abnormal sexual traits
hemophilia
mild mental impairment
hemophilia
minimal abnormalities
hemophilia
codominance
hemophilia
pleiotropy
hemophilia
epistasis
hemophilia
incomplete dominance
hemophilia
continuous variation
Down syndrome
autosomal recessive disorder
Down syndrome
X-linked disorder
Down syndrome
autosomal dominant disorder
Down syndrome
mental impairment and heart defects
Down syndrome
Sterility and mental impairment
Down syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Down syndrome
mild mental impairment
Down syndrome
minimal abnormalities
Down syndrome
codominance
Down syndrome
pleiotropy
Down syndrome
epistasis
Down syndrome
incomplete dominance
Down syndrome
continuous variation
Turner syndrome
autosomal recessive disorder
Turner syndrome
X-linked disorder
Turner syndrome
autosomal dominant disorder
Turner syndrome
mental impairment and heart defects
Turner syndrome
Sterility and mental impairment
Turner syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Turner syndrome
mild mental impairment
Turner syndrome
minimal abnormalities
Turner syndrome
codominance
Turner syndrome
pleiotropy
Turner syndrome
epistasis
Turner syndrome
incomplete dominance
Turner syndrome
continuous variation
XYY syndrome
autosomal recessive disorder
XYY syndrome
X-linked disorder
XYY syndrome
autosomal dominant disorder
XYY syndrome
mental impairment and heart defects
XYY syndrome
Sterility and mental impairment
XYY syndrome
sterility, abnormal ovaries, and abnormal sexual traits
XYY syndrome
mild mental impairment
XYY syndrome
minimal abnormalities
XYY syndrome
codominance
XYY syndrome
pleiotropy
XYY syndrome
epistasis
XYY syndrome
incomplete dominance
XYY syndrome
continuous variation
cystic fibrosis
autosomal recessive disorder
cystic fibrosis
X-linked disorder
cystic fibrosis
autosomal dominant disorder
cystic fibrosis
mental impairment and heart defects
cystic fibrosis
Sterility and mental impairment
cystic fibrosis
sterility, abnormal ovaries, and abnormal sexual traits
cystic fibrosis
mild mental impairment
cystic fibrosis
minimal abnormalities
cystic fibrosis
codominance
cystic fibrosis
pleiotropy
cystic fibrosis
epistasis
cystic fibrosis
incomplete dominance
cystic fibrosis
continuous variation
snapdragon flower color
autosomal recessive disorder
snapdragon flower color
X-linked disorder
snapdragon flower color
autosomal dominant disorder
snapdragon flower color
mental impairment and heart defects
snapdragon flower color
Sterility and mental impairment
snapdragon flower color
sterility, abnormal ovaries, and abnormal sexual traits
snapdragon flower color
mild mental impairment
snapdragon flower color
minimal abnormalities
snapdragon flower color
codominance
snapdragon flower color
pleiotropy
snapdragon flower color
epistasis
snapdragon flower color
incomplete dominance
snapdragon flower color
continuous variation
ABO blood types in humans
autosomal recessive disorder
ABO blood types in humans
X-linked disorder
ABO blood types in humans
autosomal dominant disorder
ABO blood types in humans
mental impairment and heart defects
ABO blood types in humans
Sterility and mental impairment
ABO blood types in humans
sterility, abnormal ovaries, and abnormal sexual traits
ABO blood types in humans
mild mental impairment
ABO blood types in humans
minimal abnormalities
ABO blood types in humans
codominance
ABO blood types in humans
pleiotropy
ABO blood types in humans
epistasis
ABO blood types in humans
incomplete dominance
ABO blood types in humans
continuous variation
autosomal recessive disorder
X-linked disorder
autosomal dominant disorder
mental impairment and heart defects
Sterility and mental impairment
sterility, abnormal ovaries, and abnormal sexual traits
mild mental impairment
minimal abnormalities
codominance
pleiotropy
epistasis
incomplete dominance
continuous variation
autosomal recessive disorder
X-linked disorder
autosomal dominant disorder
mental impairment and heart defects
Sterility and mental impairment
sterility, abnormal ovaries, and abnormal sexual traits
mild mental impairment
minimal abnormalities
codominance
pleiotropy
epistasis
incomplete dominance
continuous variation
Question
Suppose a single nondisjunction event occurs during anaphase II of meiosis in a normal male cell from meiosis I. Of the resulting sperm, ____.

A) three would be normal and one would have an extra chromosome
B) two would be normal, one would have an extra chromosome, and one would be missing a chromosome
C) two would have an extra chromosome and two would be missing a chromosome
D) all four sperm would have an extra chromosome
E) three would have an extra chromosome and one would be normal
Question
Match between columns
recessive phenotype
A
recessive phenotype
E
recessive phenotype
B
recessive phenotype
D
recessive phenotype
C
genotype
A
genotype
E
genotype
B
genotype
D
genotype
C
phenotype
A
phenotype
E
phenotype
B
phenotype
D
phenotype
C
dominant phenotype
A
dominant phenotype
E
dominant phenotype
B
dominant phenotype
D
dominant phenotype
C
heterozygous
A
heterozygous
E
heterozygous
B
heterozygous
D
heterozygous
C
Question
Face length in dogs is controlled by ____.

A) a dozen alleles
B) a dozen genes
C) multiple chromosomes
D) sex-linked alleles
E) trisomies
Question
The process by which chromosomes fail to separate during meiosis is called ____.

A) aneuploidy
B) trisomy
C) monosomy
D) nondisjunction
E) polyploidy
Question
Amniocentesis involves sampling ____.

A) the embryo at the eight-cell stage
B) fetal cells in the amniotic fluid
C) sperm or egg cells
D) fetal skin tissue
E) placental cells
Question
Match between columns
the particular alleles carried by an individual
incomplete dominance
the particular alleles carried by an individual
pleiotropic
the particular alleles carried by an individual
epistasis
the particular alleles carried by an individual
codominance
the particular alleles carried by an individual
genotype
the particular alleles carried by an individual
heterozygous
the particular alleles carried by an individual
dihybrid cross
the particular alleles carried by an individual
continuous variation
the particular alleles carried by an individual
syndrome
the particular alleles carried by an individual
aneuploidy
a range of small differences in a shared trait
incomplete dominance
a range of small differences in a shared trait
pleiotropic
a range of small differences in a shared trait
epistasis
a range of small differences in a shared trait
codominance
a range of small differences in a shared trait
genotype
a range of small differences in a shared trait
heterozygous
a range of small differences in a shared trait
dihybrid cross
a range of small differences in a shared trait
continuous variation
a range of small differences in a shared trait
syndrome
a range of small differences in a shared trait
aneuploidy
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
incomplete dominance
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
pleiotropic
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
epistasis
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
codominance
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
genotype
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
heterozygous
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
dihybrid cross
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
continuous variation
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
syndrome
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
aneuploidy
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
incomplete dominance
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
pleiotropic
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
epistasis
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
codominance
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
genotype
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
heterozygous
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
dihybrid cross
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
continuous variation
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
syndrome
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
aneuploidy
refers to two alleles that are both fully expressed in heterozygous individuals
incomplete dominance
refers to two alleles that are both fully expressed in heterozygous individuals
pleiotropic
refers to two alleles that are both fully expressed in heterozygous individuals
epistasis
refers to two alleles that are both fully expressed in heterozygous individuals
codominance
refers to two alleles that are both fully expressed in heterozygous individuals
genotype
refers to two alleles that are both fully expressed in heterozygous individuals
heterozygous
refers to two alleles that are both fully expressed in heterozygous individuals
dihybrid cross
refers to two alleles that are both fully expressed in heterozygous individuals
continuous variation
refers to two alleles that are both fully expressed in heterozygous individuals
syndrome
refers to two alleles that are both fully expressed in heterozygous individuals
aneuploidy
refers to a gene whose product influences multiple genes
incomplete dominance
refers to a gene whose product influences multiple genes
pleiotropic
refers to a gene whose product influences multiple genes
epistasis
refers to a gene whose product influences multiple genes
codominance
refers to a gene whose product influences multiple genes
genotype
refers to a gene whose product influences multiple genes
heterozygous
refers to a gene whose product influences multiple genes
dihybrid cross
refers to a gene whose product influences multiple genes
continuous variation
refers to a gene whose product influences multiple genes
syndrome
refers to a gene whose product influences multiple genes
aneuploidy
experiment in which individuals who have different alleles for two genes are crossed
incomplete dominance
experiment in which individuals who have different alleles for two genes are crossed
pleiotropic
experiment in which individuals who have different alleles for two genes are crossed
epistasis
experiment in which individuals who have different alleles for two genes are crossed
codominance
experiment in which individuals who have different alleles for two genes are crossed
genotype
experiment in which individuals who have different alleles for two genes are crossed
heterozygous
experiment in which individuals who have different alleles for two genes are crossed
dihybrid cross
experiment in which individuals who have different alleles for two genes are crossed
continuous variation
experiment in which individuals who have different alleles for two genes are crossed
syndrome
experiment in which individuals who have different alleles for two genes are crossed
aneuploidy
two different alleles of a given gene
incomplete dominance
two different alleles of a given gene
pleiotropic
two different alleles of a given gene
epistasis
two different alleles of a given gene
codominance
two different alleles of a given gene
genotype
two different alleles of a given gene
heterozygous
two different alleles of a given gene
dihybrid cross
two different alleles of a given gene
continuous variation
two different alleles of a given gene
syndrome
two different alleles of a given gene
aneuploidy
the set of symptoms that characterize a genetic disease
incomplete dominance
the set of symptoms that characterize a genetic disease
pleiotropic
the set of symptoms that characterize a genetic disease
epistasis
the set of symptoms that characterize a genetic disease
codominance
the set of symptoms that characterize a genetic disease
genotype
the set of symptoms that characterize a genetic disease
heterozygous
the set of symptoms that characterize a genetic disease
dihybrid cross
the set of symptoms that characterize a genetic disease
continuous variation
the set of symptoms that characterize a genetic disease
syndrome
the set of symptoms that characterize a genetic disease
aneuploidy
effect in which a trait is influenced by the product of multiple genes
incomplete dominance
effect in which a trait is influenced by the product of multiple genes
pleiotropic
effect in which a trait is influenced by the product of multiple genes
epistasis
effect in which a trait is influenced by the product of multiple genes
codominance
effect in which a trait is influenced by the product of multiple genes
genotype
effect in which a trait is influenced by the product of multiple genes
heterozygous
effect in which a trait is influenced by the product of multiple genes
dihybrid cross
effect in which a trait is influenced by the product of multiple genes
continuous variation
effect in which a trait is influenced by the product of multiple genes
syndrome
effect in which a trait is influenced by the product of multiple genes
aneuploidy
Question
____ is an example of a genetic disorder with little impact on the individual.

A) XXX syndrome
B) Turner syndrome
C) Hemophilia
D) XYY syndrome
E) Down syndrome
Question
Genetic testing by ____ can be performed earliest in pregnancy.

A) amniocentesis
B) obstetric sonography
C) fetoscopy
D) chorionic villus sampling
E) preimplantation genetic diagnosis
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Deck 10: Patterns of Inheritance
1
When two alleles of the same gene are identical, the individual carrying those alleles is said to be ____.

A) dominant
B) heterozygous
C) recessive
D) genotypical
E) homozygous
E
2
An allele is ____ if its effect masks that of a ____ allele paired with it.

A) recessive; codominant
B) codominant; recessive
C) recessive; dominant
D) dominant; recessive
E) incompletely recessive; dominant
D
3
Observable traits are known in genetics as ____.

A) phenotypes
B) genotypes
C) homozygous
D) heterozygous
E) homozygous genotypes
A
4
In cats, short hair ( L ) is dominant to long hair ( l ). If a short-haired cat of unknown genotype is crossed with a long-haired animal, and they produce one long-haired kitten and one short-haired kitten, this would indicate that ____.

A) the short-haired cat was true-breeding
B) the short-haired cat was not true-breeding
C) the long-haired cat was not true-breeding
D) the long-haired cat was heterozygous
E) neither parent was true-breeding
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5
In a person with cystic fibrosis, the CFTR mutation causes the protein to be ____.

A) embedded in the plasma membrane
B) destroyed in the endoplasmic reticulum
C) shuttled to the nuclear membrane instead of the plasma membrane
D) shuttled to the plasma membrane instead of the nuclear membrane
E) expelled from the cell by exocytosis before it can do its job
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6
Various forms of the same gene are called ____.

A) genotypes
B) alleles
C) somatic
D) recessive
E) phenotypes
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7
Red coat is dominant in horses and white coat is recessive. In a cross between a homozygous dominant red-coated horse and a white-coated horse, what genotype(s) would be observed in the offspring?

A) all homozygous recessive
B) all homozygous dominant
C) half homozygous dominant and half homozygous recessive
D) all heterozygous
E) half heterozygous and half homozygous dominant
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8
____ raises miscarriage risks by 2-10 percent and is rarely performed.

A) Conventional ultrasound
B) Fetoscopy
C) 4D ultrasound
D) Amniocentesis
E) CVS
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9
The mutated gene that causes cystic fibrosis is ____.

A) CFTR
B) CRFT
C) CTFR
D) CRTF
E) CFRT
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10
When Gregor Mendel first started his genetics experiments, he ____.

A) knew about the existence of genes
B) knew that some plants "breed true"
C) knew that genes were responsible for observable traits
D) allowed the pea plants to self-fertilize
E) expected all true breeding crosses to produce offspring with intermediate phenotypes
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11
When two alleles of the same gene are different, the individual carrying those alleles is said to be ____.

A) recessive
B) heterozygous
C) phenotypic
D) somatic
E) homozygous
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12
The most common type of mutation that causes cystic fibrosis is a(n) ____.

A) deletion
B) insertion
C) base-pair substitution
D) gene duplication
E) transformation
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13
The failure of which organ affected by a defective CFTR protein is likely to cause death in cystic fibrosis patients?

A) lungs
B) intestines
C) heart
D) liver
E) reproductive system
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14
If R is dominant to r , the offspring of the cross of RR with rr will ____.

A) have a unique phenotype
B) have the same phenotype as the RR parents
C) have the same phenotype as the rr parents
D) have the same genotype as the RR parents
E) have the same genotype as the rr parents
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15
An individual's ____ determines its observable ____.

A) phenotype; genotype
B) genotype; phenotype
C) gene location; allele
D) heterozygote; homozygote
E) homozygote; heterozygote
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16
If tall ( D ) is dominant to dwarf ( d ), and two homozygous varieties DD and dd are crossed, the progeny produced will be____.

A) all intermediate forms
B) all tall
C) all dwarf
D) 1/2 tall and 1/2 dwarf
E) 3/4 tall and 1/4 dwarf
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17
____ is the most fatal genetic disorder in the United States.

A) Cystic fibrosis
B) Huntington's disease
C) Sickle-cell anemia
D) Anhidrotic dysplasia
E) Color blindness
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18
In the lungs of cystic fibrosis patients, ____.

A) chloride ions are stuck inside epithelial cells
B) water is excessively abundant on epithelial surfaces
C) epithelial surfaces are coated with slippery mucus
D) excess water and chloride ions are pumped out of epithelial cells
E) chloride ions are not transported out of epithelial cells, and epithelial surfaces are dry
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19
The main problem for those with cystic fibrosis involves ____.

A) mucus sticking to dry surfaces
B) jerky muscle contractions
C) constant thirst
D) salt accumulations between tissues
E) low pH in tissues preventing proper enzymatic activity
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20
A(n) ____ is an offspring of a cross between two individuals that breed true for different forms of a given trait.

A) homozygote
B) recessive
C) hybrid
D) phenotype
E) genotype
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21
The mutation that causes the lighter skin color of all people of European descent was the result of a ____ in the gene for a melanin transport protein.

A) base-pair substitution
B) insertion
C) deletion
D) whole chromosome duplication
E) multiple gene mutations involving several mechanisms
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22
Genetic recombination as a result of crossing over occurs more readily between genes that are ____.

A) on the sex chromosomes
B) near the centromere
C) located close together on the same chromosome
D) located far apart on the same chromosome
E) located on different chromosomes
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23
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, how many plants would have white flowers and short stems?</strong> A) 1 B) 3 C) 5 D) 9 E) 16 Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, how many plants would have white flowers and short stems?

A) 1
B) 3
C) 5
D) 9
E) 16
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24
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( A aBb   ´   AaBb ). In the figure above, how many plants would have purple flowers and tall stems?</strong> A) 1 B) 3 C) 5 D) 9 E) 16 Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( A aBb   ´   AaBb ).
In the figure above, how many plants would have purple flowers and tall stems?

A) 1
B) 3
C) 5
D) 9
E) 16
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25
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, what would be the genotype of plant #7?</strong> A) AaBb B) AABb C) AaBB D) AABB E) aaBB Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, what would be the genotype of plant #7?

A) AaBb
B) AABb
C) AaBB
D) AABB
E) aaBB
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26
For this problem, you may want to create a Punnett Square on a separate piece of paper. Manuel has cystic fibrosis, a recessive disorder, and sickle-cell anemia, which is also a recessive disorder. Manuel's partner, Lucretia, is normal for both conditions. What is the probability that Manuel and Lucretia will have a normal child without either of the conditions Manuel has?

A) 0  percent
B) 25  percent
C) 75  percent
D) 100  percent
E) It is not possible to solve this problem with the information provided.
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27
In cats, short hair L is dominant to long hair l and black hair B is dominant to brown hair b . If you found a black, short-haired cat, you could determine his genotype by crossing it to an animal with a genotype of ____.

A) LLBB
B) llBB
C) llBb
D) llbb
E) LLbb
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28
If two individuals who are heterozygous for two traits that display incomplete dominance (e.g., AaBb) mate and have offspring, how many different phenotypes are possible?

A) 1
B) 3
C) 6
D) 9
E) 16
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29
Cystic fibrosis is a recessive disorder. If a couple, each of whom is heterozygous for the CFTR mutation, have children, what is the probability that they will have a child with cystic fibrosis?

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
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30
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, what would be the genotype of plant #9?</strong> A) Aabb B) aaBb C) AaBB D) AABB E) aaBB Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, what would be the genotype of plant #9?

A) Aabb
B) aaBb
C) AaBB
D) AABB
E) aaBB
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31
The ease of detecting and treating ____ is a good example of the advantages of genetic screening.

A) PKU
B) Tay-Sachs
C) Marfan syndrome
D) color blindness
E) Down syndrome
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32
The discarded theory of blending inheritance most closely resembles ____.

A) X-linked inheritance
B) dihybridization
C) codominance
D) incomplete dominance
E) complete dominance
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33
If a child has an AB blood type, ____.

A) both parents must have different blood types
B) neither parent can have blood type AB
C) both parents must have blood type AB
D) both parents can be any blood type
E) one parent can have blood type O
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34
In a Punnett square, the letters on top of the square and on the side of the square represent ____.

A) offspring genotypes
B) zygote genotypes
C) parental gametes
D) offspring phenotypes
E) parental phenotypes
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35
For this problem, you may want to create a Punnett Square on a separate piece of paper. Assume brown eyes are dominant to blue eyes and dimples are dominant to no dimples. John has brown eyes, and his mother has blue eyes. John does not have dimples. Zena has blue eyes and also has no dimples. What are the chances if this couple have children, they will produce a child with blue eyes and no dimples?

A) 0
B) ¼
C) ½
D) ¾
E) There is not enough information provided to solve this problem.
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36
In codominance, ____.

A) one allele is dominant to another allele
B) the genotype is determined by the phenotype
C) the heterozygous phenotype is intermediate to the homozygous phenotypes
D) the intermediate phenotype may be the result of enzyme insufficiency
E) two alleles may be equally expressed
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37
Approximately how many gene products are involved in the synthesis of melanin in humans?

A) 10
B) 25
C) 50
D) 100
E) 1000
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38
<strong>  Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ). In the figure above, how many plants would have the genotype AaBb ?</strong> A) 1 B) 3 C) 4 D) 6 E) 9 Purple flower ( A ) is dominant over white flower ( a ), and tall stem ( B ) is dominant over short stem ( b ). The Punnett square represents a cross between two dihybrids ( AaBb   ´   AaBb ).
In the figure above, how many plants would have the genotype AaBb ?

A) 1
B) 3
C) 4
D) 6
E) 9
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39
In a cross of a DDRR individual with a ddrr individual, the genotype of all offspring will ____.

A) DDRR
B) DdRR
C) DdRr
D) ddRR
E) ddRr
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40
If a pure-breeding wired-hair terrier ( WW ) is crossed with a pure-breeding smooth-hair terrier (ww), and a puppy with a wavy hair is produced, the simplest explanation is ____.

A) a mutation has occurred
B) hair texture is an X-linked trait
C) incomplete dominance
D) hair texture is a lethal trait
E) codominance
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41
When genes are located very close together on the same chromosome, ____.

A) gametes usually end up with the same combination of alleles as parental cells
B) gametes usually end up with unique combination of alleles
C) they are inherited separately
D) they often recombine during crossing over
E) offspring will look just like one parent
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42
The switching between asexual and sexual reproduction by water fleas is controlled by ____.

A) epistasis
B) pleiotropy
C) incomplete dominance
D) codominant inheritance
E) environmental effects
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43
In an autosomal dominant disorder such as Huntington's disease, two carrier parents have the probability of passing the gene onto ____ of their children.

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
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44
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is the probability that they will be normal?

A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
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45
In a pedigree chart, a male who demonstrates the trait being studied is represented by a ____.

A) darkened square
B) darkened diamond
C) clear circle
D) clear square
E) darkened circle
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46
Narrative:
Achondroplasia, a hereditary form of dwarfism, is an autosomal dominant disorder; however homozygous dominant individuals either die before birth or very shortly thereafter. The homozygous recessive condition is normal. A dwarf couple decide to have children. Use this information to answer the following question:
Of the children of this couple who survive, what is probability that they will be affected by achondroplasia?

A) 0
B) ¼
C) 1/3
D) 2/3
E) ½
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47
In the Bombay phenotype, a gene in the recessive condition blocks the expression of A and B red blood cell antigens. Thus, all A, B, and AB genotypes are expressed as the O phenotype. This is an example of ____.

A) complete dominance
B) polygeny
C) incomplete dominance
D) codominance
E) pleiotropy
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48
A gene that produces multiple effects is called a(n) ____.

A) codominant gene
B) X-linked gene
C) epistatic gene
D) pleiotropic gene
E) incompletely dominant gene
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49
A pleiotropic gene ____.

A) acts on secondary sexual characteristics
B) influences multiple traits
C) is additive
D) produces lethal effects when homozygous
E) produces epigenetic effects
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50
The probability of producing a normal child by two parents who are carriers for an autosomal recessive disorder is ____.

A) 0  percent
B) 25  percent
C) 50  percent
D) 75  percent
E) 100  percent
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51
An X-linked carrier is a ____.

A) homozygous dominant female
B) heterozygous female
C) homozygous recessive female
D) homozygous male
E) heterozygous male
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52
Geneticists use ____ to study the genetics of families through generations.

A) Punnett squares
B) pedigrees
C) karyotypes
D) DNA profiles
E) fossil analyses
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53
The ABO blood types have ____ different genotypes.

A) 4
B) 6
C) 8
D) 12
E) 16
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54
An autosomal recessive disorder ____.

A) requires that only one parent be a carrier
B) displays its symptoms in heterozygotes
C) is more frequent in males than females
D) requires that both parents are carriers
E) only affects females
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55
Human eye color is an example of a trait that varies ____.

A) according to the geographical area
B) periodically
C) according to humidity
D) continuously
E) according to seasons
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56
In humans, skin color is controlled by several genes. Thus, skin color is a(n) ____ characteristic.

A) dominant
B) codominant
C) polygenic
D) pleiotropic
E) recessive
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57
In a pedigree chart, a female showing the specific trait being studied is indicated by a ____.

A) clear square
B) darkened square
C) clear circle
D) darkened diamond
E) darkened circle
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58
Six fingers on one hand would be classified as a(n) ____.

A) genetic disorder
B) disease
C) syndrome
D) genetic abnormality
E) illness
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59
In Siamese cats, enzymes that code for dark fur color are only active in cooler temperatures. Thus, the tips of a Siamese cat's ears, feet, and tail are dark but not the warmer regions of its body core. This is an example of ____.

A) p leiotropy
B) environmental effects
C) epistasis
D) incomplete dominance
E) codominance
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60
Males are more commonly affected by X-linked recessive genetic disorders than females because ____.

A) females have two X chromosomes; therefore, they do not inherit recessive alleles
B) males have only one X chromosome; therefore, they express all recessive X-linked traits
C) males have only one X chromosome; therefore, they have multiple alleles for each X-linked gene
D) Y chromosomes cause X-linked gene mutations
E) males are genetically weaker than females
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61
Match between columns
polydactyly
autosomal recessive disorder
polydactyly
X-linked disorder
polydactyly
autosomal dominant disorder
polydactyly
mental impairment and heart defects
polydactyly
Sterility and mental impairment
polydactyly
sterility, abnormal ovaries, and abnormal sexual traits
polydactyly
mild mental impairment
polydactyly
minimal abnormalities
polydactyly
codominance
polydactyly
pleiotropy
polydactyly
epistasis
polydactyly
incomplete dominance
polydactyly
continuous variation
XXX syndrome
autosomal recessive disorder
XXX syndrome
X-linked disorder
XXX syndrome
autosomal dominant disorder
XXX syndrome
mental impairment and heart defects
XXX syndrome
Sterility and mental impairment
XXX syndrome
sterility, abnormal ovaries, and abnormal sexual traits
XXX syndrome
mild mental impairment
XXX syndrome
minimal abnormalities
XXX syndrome
codominance
XXX syndrome
pleiotropy
XXX syndrome
epistasis
XXX syndrome
incomplete dominance
XXX syndrome
continuous variation
Marfan syndrome
autosomal recessive disorder
Marfan syndrome
X-linked disorder
Marfan syndrome
autosomal dominant disorder
Marfan syndrome
mental impairment and heart defects
Marfan syndrome
Sterility and mental impairment
Marfan syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Marfan syndrome
mild mental impairment
Marfan syndrome
minimal abnormalities
Marfan syndrome
codominance
Marfan syndrome
pleiotropy
Marfan syndrome
epistasis
Marfan syndrome
incomplete dominance
Marfan syndrome
continuous variation
fur color in Labrador retrievers
autosomal recessive disorder
fur color in Labrador retrievers
X-linked disorder
fur color in Labrador retrievers
autosomal dominant disorder
fur color in Labrador retrievers
mental impairment and heart defects
fur color in Labrador retrievers
Sterility and mental impairment
fur color in Labrador retrievers
sterility, abnormal ovaries, and abnormal sexual traits
fur color in Labrador retrievers
mild mental impairment
fur color in Labrador retrievers
minimal abnormalities
fur color in Labrador retrievers
codominance
fur color in Labrador retrievers
pleiotropy
fur color in Labrador retrievers
epistasis
fur color in Labrador retrievers
incomplete dominance
fur color in Labrador retrievers
continuous variation
Klinefelter syndrome
autosomal recessive disorder
Klinefelter syndrome
X-linked disorder
Klinefelter syndrome
autosomal dominant disorder
Klinefelter syndrome
mental impairment and heart defects
Klinefelter syndrome
Sterility and mental impairment
Klinefelter syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Klinefelter syndrome
mild mental impairment
Klinefelter syndrome
minimal abnormalities
Klinefelter syndrome
codominance
Klinefelter syndrome
pleiotropy
Klinefelter syndrome
epistasis
Klinefelter syndrome
incomplete dominance
Klinefelter syndrome
continuous variation
height in humans
autosomal recessive disorder
height in humans
X-linked disorder
height in humans
autosomal dominant disorder
height in humans
mental impairment and heart defects
height in humans
Sterility and mental impairment
height in humans
sterility, abnormal ovaries, and abnormal sexual traits
height in humans
mild mental impairment
height in humans
minimal abnormalities
height in humans
codominance
height in humans
pleiotropy
height in humans
epistasis
height in humans
incomplete dominance
height in humans
continuous variation
hemophilia
autosomal recessive disorder
hemophilia
X-linked disorder
hemophilia
autosomal dominant disorder
hemophilia
mental impairment and heart defects
hemophilia
Sterility and mental impairment
hemophilia
sterility, abnormal ovaries, and abnormal sexual traits
hemophilia
mild mental impairment
hemophilia
minimal abnormalities
hemophilia
codominance
hemophilia
pleiotropy
hemophilia
epistasis
hemophilia
incomplete dominance
hemophilia
continuous variation
Down syndrome
autosomal recessive disorder
Down syndrome
X-linked disorder
Down syndrome
autosomal dominant disorder
Down syndrome
mental impairment and heart defects
Down syndrome
Sterility and mental impairment
Down syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Down syndrome
mild mental impairment
Down syndrome
minimal abnormalities
Down syndrome
codominance
Down syndrome
pleiotropy
Down syndrome
epistasis
Down syndrome
incomplete dominance
Down syndrome
continuous variation
Turner syndrome
autosomal recessive disorder
Turner syndrome
X-linked disorder
Turner syndrome
autosomal dominant disorder
Turner syndrome
mental impairment and heart defects
Turner syndrome
Sterility and mental impairment
Turner syndrome
sterility, abnormal ovaries, and abnormal sexual traits
Turner syndrome
mild mental impairment
Turner syndrome
minimal abnormalities
Turner syndrome
codominance
Turner syndrome
pleiotropy
Turner syndrome
epistasis
Turner syndrome
incomplete dominance
Turner syndrome
continuous variation
XYY syndrome
autosomal recessive disorder
XYY syndrome
X-linked disorder
XYY syndrome
autosomal dominant disorder
XYY syndrome
mental impairment and heart defects
XYY syndrome
Sterility and mental impairment
XYY syndrome
sterility, abnormal ovaries, and abnormal sexual traits
XYY syndrome
mild mental impairment
XYY syndrome
minimal abnormalities
XYY syndrome
codominance
XYY syndrome
pleiotropy
XYY syndrome
epistasis
XYY syndrome
incomplete dominance
XYY syndrome
continuous variation
cystic fibrosis
autosomal recessive disorder
cystic fibrosis
X-linked disorder
cystic fibrosis
autosomal dominant disorder
cystic fibrosis
mental impairment and heart defects
cystic fibrosis
Sterility and mental impairment
cystic fibrosis
sterility, abnormal ovaries, and abnormal sexual traits
cystic fibrosis
mild mental impairment
cystic fibrosis
minimal abnormalities
cystic fibrosis
codominance
cystic fibrosis
pleiotropy
cystic fibrosis
epistasis
cystic fibrosis
incomplete dominance
cystic fibrosis
continuous variation
snapdragon flower color
autosomal recessive disorder
snapdragon flower color
X-linked disorder
snapdragon flower color
autosomal dominant disorder
snapdragon flower color
mental impairment and heart defects
snapdragon flower color
Sterility and mental impairment
snapdragon flower color
sterility, abnormal ovaries, and abnormal sexual traits
snapdragon flower color
mild mental impairment
snapdragon flower color
minimal abnormalities
snapdragon flower color
codominance
snapdragon flower color
pleiotropy
snapdragon flower color
epistasis
snapdragon flower color
incomplete dominance
snapdragon flower color
continuous variation
ABO blood types in humans
autosomal recessive disorder
ABO blood types in humans
X-linked disorder
ABO blood types in humans
autosomal dominant disorder
ABO blood types in humans
mental impairment and heart defects
ABO blood types in humans
Sterility and mental impairment
ABO blood types in humans
sterility, abnormal ovaries, and abnormal sexual traits
ABO blood types in humans
mild mental impairment
ABO blood types in humans
minimal abnormalities
ABO blood types in humans
codominance
ABO blood types in humans
pleiotropy
ABO blood types in humans
epistasis
ABO blood types in humans
incomplete dominance
ABO blood types in humans
continuous variation
autosomal recessive disorder
X-linked disorder
autosomal dominant disorder
mental impairment and heart defects
Sterility and mental impairment
sterility, abnormal ovaries, and abnormal sexual traits
mild mental impairment
minimal abnormalities
codominance
pleiotropy
epistasis
incomplete dominance
continuous variation
autosomal recessive disorder
X-linked disorder
autosomal dominant disorder
mental impairment and heart defects
Sterility and mental impairment
sterility, abnormal ovaries, and abnormal sexual traits
mild mental impairment
minimal abnormalities
codominance
pleiotropy
epistasis
incomplete dominance
continuous variation
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62
Suppose a single nondisjunction event occurs during anaphase II of meiosis in a normal male cell from meiosis I. Of the resulting sperm, ____.

A) three would be normal and one would have an extra chromosome
B) two would be normal, one would have an extra chromosome, and one would be missing a chromosome
C) two would have an extra chromosome and two would be missing a chromosome
D) all four sperm would have an extra chromosome
E) three would have an extra chromosome and one would be normal
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63
Match between columns
recessive phenotype
A
recessive phenotype
E
recessive phenotype
B
recessive phenotype
D
recessive phenotype
C
genotype
A
genotype
E
genotype
B
genotype
D
genotype
C
phenotype
A
phenotype
E
phenotype
B
phenotype
D
phenotype
C
dominant phenotype
A
dominant phenotype
E
dominant phenotype
B
dominant phenotype
D
dominant phenotype
C
heterozygous
A
heterozygous
E
heterozygous
B
heterozygous
D
heterozygous
C
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64
Face length in dogs is controlled by ____.

A) a dozen alleles
B) a dozen genes
C) multiple chromosomes
D) sex-linked alleles
E) trisomies
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65
The process by which chromosomes fail to separate during meiosis is called ____.

A) aneuploidy
B) trisomy
C) monosomy
D) nondisjunction
E) polyploidy
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66
Amniocentesis involves sampling ____.

A) the embryo at the eight-cell stage
B) fetal cells in the amniotic fluid
C) sperm or egg cells
D) fetal skin tissue
E) placental cells
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67
Match between columns
the particular alleles carried by an individual
incomplete dominance
the particular alleles carried by an individual
pleiotropic
the particular alleles carried by an individual
epistasis
the particular alleles carried by an individual
codominance
the particular alleles carried by an individual
genotype
the particular alleles carried by an individual
heterozygous
the particular alleles carried by an individual
dihybrid cross
the particular alleles carried by an individual
continuous variation
the particular alleles carried by an individual
syndrome
the particular alleles carried by an individual
aneuploidy
a range of small differences in a shared trait
incomplete dominance
a range of small differences in a shared trait
pleiotropic
a range of small differences in a shared trait
epistasis
a range of small differences in a shared trait
codominance
a range of small differences in a shared trait
genotype
a range of small differences in a shared trait
heterozygous
a range of small differences in a shared trait
dihybrid cross
a range of small differences in a shared trait
continuous variation
a range of small differences in a shared trait
syndrome
a range of small differences in a shared trait
aneuploidy
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
incomplete dominance
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
pleiotropic
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
epistasis
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
codominance
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
genotype
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
heterozygous
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
dihybrid cross
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
continuous variation
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
syndrome
condition in which one allele is not fully dominant over another; the heterozygous phenotype appears to be a blend of the two homozygous phenotypes
aneuploidy
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
incomplete dominance
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
pleiotropic
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
epistasis
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
codominance
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
genotype
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
heterozygous
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
dihybrid cross
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
continuous variation
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
syndrome
a chromosome abnormality in which there are too many or too few copies of a particular chromosome
aneuploidy
refers to two alleles that are both fully expressed in heterozygous individuals
incomplete dominance
refers to two alleles that are both fully expressed in heterozygous individuals
pleiotropic
refers to two alleles that are both fully expressed in heterozygous individuals
epistasis
refers to two alleles that are both fully expressed in heterozygous individuals
codominance
refers to two alleles that are both fully expressed in heterozygous individuals
genotype
refers to two alleles that are both fully expressed in heterozygous individuals
heterozygous
refers to two alleles that are both fully expressed in heterozygous individuals
dihybrid cross
refers to two alleles that are both fully expressed in heterozygous individuals
continuous variation
refers to two alleles that are both fully expressed in heterozygous individuals
syndrome
refers to two alleles that are both fully expressed in heterozygous individuals
aneuploidy
refers to a gene whose product influences multiple genes
incomplete dominance
refers to a gene whose product influences multiple genes
pleiotropic
refers to a gene whose product influences multiple genes
epistasis
refers to a gene whose product influences multiple genes
codominance
refers to a gene whose product influences multiple genes
genotype
refers to a gene whose product influences multiple genes
heterozygous
refers to a gene whose product influences multiple genes
dihybrid cross
refers to a gene whose product influences multiple genes
continuous variation
refers to a gene whose product influences multiple genes
syndrome
refers to a gene whose product influences multiple genes
aneuploidy
experiment in which individuals who have different alleles for two genes are crossed
incomplete dominance
experiment in which individuals who have different alleles for two genes are crossed
pleiotropic
experiment in which individuals who have different alleles for two genes are crossed
epistasis
experiment in which individuals who have different alleles for two genes are crossed
codominance
experiment in which individuals who have different alleles for two genes are crossed
genotype
experiment in which individuals who have different alleles for two genes are crossed
heterozygous
experiment in which individuals who have different alleles for two genes are crossed
dihybrid cross
experiment in which individuals who have different alleles for two genes are crossed
continuous variation
experiment in which individuals who have different alleles for two genes are crossed
syndrome
experiment in which individuals who have different alleles for two genes are crossed
aneuploidy
two different alleles of a given gene
incomplete dominance
two different alleles of a given gene
pleiotropic
two different alleles of a given gene
epistasis
two different alleles of a given gene
codominance
two different alleles of a given gene
genotype
two different alleles of a given gene
heterozygous
two different alleles of a given gene
dihybrid cross
two different alleles of a given gene
continuous variation
two different alleles of a given gene
syndrome
two different alleles of a given gene
aneuploidy
the set of symptoms that characterize a genetic disease
incomplete dominance
the set of symptoms that characterize a genetic disease
pleiotropic
the set of symptoms that characterize a genetic disease
epistasis
the set of symptoms that characterize a genetic disease
codominance
the set of symptoms that characterize a genetic disease
genotype
the set of symptoms that characterize a genetic disease
heterozygous
the set of symptoms that characterize a genetic disease
dihybrid cross
the set of symptoms that characterize a genetic disease
continuous variation
the set of symptoms that characterize a genetic disease
syndrome
the set of symptoms that characterize a genetic disease
aneuploidy
effect in which a trait is influenced by the product of multiple genes
incomplete dominance
effect in which a trait is influenced by the product of multiple genes
pleiotropic
effect in which a trait is influenced by the product of multiple genes
epistasis
effect in which a trait is influenced by the product of multiple genes
codominance
effect in which a trait is influenced by the product of multiple genes
genotype
effect in which a trait is influenced by the product of multiple genes
heterozygous
effect in which a trait is influenced by the product of multiple genes
dihybrid cross
effect in which a trait is influenced by the product of multiple genes
continuous variation
effect in which a trait is influenced by the product of multiple genes
syndrome
effect in which a trait is influenced by the product of multiple genes
aneuploidy
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68
____ is an example of a genetic disorder with little impact on the individual.

A) XXX syndrome
B) Turner syndrome
C) Hemophilia
D) XYY syndrome
E) Down syndrome
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69
Genetic testing by ____ can be performed earliest in pregnancy.

A) amniocentesis
B) obstetric sonography
C) fetoscopy
D) chorionic villus sampling
E) preimplantation genetic diagnosis
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Unlock Deck
Unlock for access to all 69 flashcards in this deck.