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Mendel called physical units responsible for the inheritance of traits "characters." The basis for his first law is that characters


A) separate from each other during meiosis.
B) are carried on separate chromosomes.
C) can exist as multiple alleles.
D) are inherited in random combinations.
E) can be cloned using nuclear transfer.

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In the Foofnagle family,the trait of being able to yodel affects members of both sexes in every generation.This trait could be


A) autosomal recessive or autosomal dominant.
B) autosomal recessive but not autosomal dominant.
C) autosomal dominant but not autosomal recessive.
D) conclusive or inconclusive.
E) caused by something in the environment and not inherited at all.

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The difference in mode of inheritance between Huntington disease and cystic fibrosis is that


A) Huntington disease only affects men and cystic fibrosis affects both sexes.
B) Huntington disease skips generations and only affects children, whereas cystic fibrosis can strike at any age and never skips generations.
C) Huntington disease does not skip generations but cystic fibrosis can.
D) A person with Huntington disease can have unaffected parents, but a person with cystic fibrosis must have an affected parent.
E) Huntington disease affects females and cystic fibrosis affects males.

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A very difficult aspect of Huntington disease is that


A) it affects different people in a family at very different ages.
B) it affects different people in a family in different parts of the body.
C) it affects different people in a family in different parts of the brain.
D) a family may include individuals at different stages of the illness.
E) the disease can become infectious, and pass even to those who do not have the mutation.

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A Punnett square displays


A) members of a family and their phenotypes.
B) paired chromosomes in size order.
C) DNA sequences and the proteins they encode.
D) the probabilities of how alleles combine in offspring.
E) only the males in a pedigree.

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When Mendel crossed pure breeding peas having yellow seed color (YY) with pure breeding peas having green seed color (yy) ,all of the offspring had yellow seed color.These results mean that yellow seed color is the


A) genotype.
B) dominant phenotype.
C) mode of inheritance.
D) recessive phenotype.
E) mutant phenotype.

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Eric and Janelle are carriers of the recessive allele causing Tay-Sachs disease,which is lethal in early childhood.If they have a healthy child,what is the probability that this child would NOT be a carrier of Tay-Sachs disease?


A) 1
B) 2/3
C) 1/2
D) 1/3
E) 78

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In a human pedigree that traces the inheritance of sickle cell disease,a half-filled circle represents a


A) male with the disease.
B) female with the disease.
C) heterozygous male.
D) heterozygous female.
E) individual who died.

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A heterozygote has


A) two different alleles for a gene.
B) two of the same alleles for a gene.
C) only one allele for a gene.
D) an extra genome.
E) one copy of each sex chromosome.

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Ian and Bryony are both carriers for two autosomal recessive disorders,PKU (chromosome 12) and cystic fibrosis (chromosome 7) .They are expecting a daughter.What is the probability that she will have PKU but not CF?


A) 3/4.
B) 9/16.
C) 3/16.
D) 1/2.
E) 1/16.

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A very narrow pedigree,such as that for Egypt's Ptolemy dynasty,reflects


A) families with many children.
B) families with many adopted children.
C) a very mild phenotype.
D) many uncles marrying their nephews.
E) families with many relatives having children with blood relatives.

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The second generation resulting from a genetic cross is the _______ generation.


A) P1
B) P2
C) F1
D) F2
E) L1

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An autosomal dominant trait


A) passes from mother to son only.
B) skips generations.
C) can be carried by unaffected individuals.
D) can affect either sex.
E) is only seen when homozygous.

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Sickle cell disease is inherited as an autosomal recessive trait.The genotype of an individual with sickle cell disease is


A) homozygous dominant.
B) homozygous recessive.
C) heterozygous dominant.
D) heterozygous recessive.
E) unable to be determined by the phenotype.

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A(n) ______ cross yields a genotypic ratio of 1:2:1 and a phenotypic ratio of 3:1.


A) allelic
B) monohybrid
C) test
D) dihybrid
E) trihybrid

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The genotypic ratio expected from a dihybrid cross involving complete dominance is


A) 3:1.
B) 1:2:1.
C) 9:3:1.
D) 9:3:3:1.
E) 4:1.

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In a human pedigree that traces the inheritance of albinism,a filled square represents a


A) male with albinism.
B) female with albinism.
C) heterozygous male.
D) heterozygous female.
E) a female who is homozygous for the wild type allele.

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Which of the following represents a monohybrid cross?


A) Bb x Bb
B) AaBb x AaBb
C) BB x bb
D) AABB x aabb
E) a x b

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In pea plants,the allele for tall (T) is dominant to the allele for short (t) .The genotype for a short pea plant is __.


A) TT
B) Tt
C) tt
D) Tt or tt
E) TT or tt

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Jaden is six years old.His sister Hillary has the autosomal recessive condition neuronal ceroid lipofuscinosis that affects learning and coordination.Their parents are healthy.The probability that Jaden is a homozygote for the wild type allele of the gene that causes the condition is


A) 1/8.
B) 1/4.
C) 1/3.
D) 2/3.
E) 0.

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