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A human cell that has 69 chromosomes is


A) aneuploid.
B) triploid.
C) diploid.
D) euploid.

E) All of the above
F) None of the above

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In von Willebrand disease, which is either autosomal recessive or autosomal dominant, clotting time slows and the person bruises and bleeds easily. Not everyone who inherits the disease genotype actually develops the phenotype. Affected individuals have differing degrees of difficulty in blood clotting. This condition is


A) completely penetrant, variably expressive, and not genetically heterogeneic.
B) incompletely penetrant, variably expressive, and genetically heterogeneic.
C) completely penetrant, invariably expressive, and not genetically heterogeneic.
D) pleiotropic and genetically heterogeneic.

E) None of the above
F) C) and D)

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A woman wishes to have her unborn child tested for genetic disorders and see a full karyotype of her child's genome but does not want to have the amniotic sac punctured to retrieve samples. Which of the following tests will give the most accurate and thorough examination of the fetal genome without puncturing the amniotic sac to retrieve fetal DNA?


A) Amniocentesis
B) Chorionic villus sampling
C) Ultrasonography
D) Maternal serum marker screening

E) B) and D)
F) C) and D)

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The human genome contains millions of different genes.

A) True
B) False

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Antonio is colorblind. His partner Emilia is not colorblind nor is she a carrier (heterozygote) for colorblindness. The offspring of this couple would


A) be sons with colorblindness and daughters with color vision.
B) be colorblind daughters and sons with normal color vision.
C) all be colorblind.
D) all have normal color vision.

E) A) and C)
F) A) and D)

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Absence of the SRY gene and expression of the Wnt4 gene are necessary for female reproductive structures to develop in an embryo and fetus.

A) True
B) False

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True

An example of a sex-influenced trait is


A) baldness.
B) hemophilia.
C) colorblindness.
D) hypertension.

E) B) and C)
F) A) and B)

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A couple is trying to calculate the chance of genetic traits in their potential offspring. From family history, the man presumes he is heterozygous for the height gene via the "tall" allele (T) . His partner is short in stature, so she believes she is homozygous for the height gene via the "short" allele (t) . Assuming the "tall" allele is completely dominant, what is the chance that their offspring would be tall in stature? 


A) 25%
B) 50%
C) 75%
D) 100%

E) B) and D)
F) A) and B)

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The origin of the 46 chromosomes in a human zygote is


A) all from the sperm cell.
B) half from DNA and half from RNA.
C) half from the sperm and half from the egg.
D) all from the egg.

E) All of the above
F) None of the above

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C

An offspring of parents whose genotypes are Aa and Aa may be


A) only Aa.
B) AA or aa.
C) AA, Aa, or aa.
D) only aa.

E) A) and C)
F) All of the above

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A karyotype is


A) a diagram that represents family relationships.
B) a size-ordered chart of chromosomes.
C) a genome sequence.
D) a website that lists genes and the proteins they encode.

E) C) and D)
F) A) and B)

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The nuances of eye color arise from


A) the numbers of rods and cones in the retina.
B) the way pigments are deposited in the iris.
C) how much vitamin A is in a person's diet.
D) multiple alleles of at least 10 genes.

E) A) and B)
F) A) and C)

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Gametes pass genetic information from generation to generation.

A) True
B) False

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The genotypes and phenotypes that result from the cross of Aa and Aa (A = normal pigmentation and a = albinism) are


A) phenotypes:75% normal and 25% albino; genotypes:25% homozygous dominant and 50% heterozygous and 25% homozygous recessive.
B) phenotypes:50% normal and 50% albino; genotypes:all homozygous recessive.
C) phenotypes:50% normal and 50% albino; genotypes:50% homozygous recessive and 50% homozygous dominant.
D) phenotypes:25% normal and 75% albino; genotypes:25% homozygous dominant and 50% heterozygous and 25% homozygous recessive.

E) A) and D)
F) C) and D)

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Most of the DNA in the human genome encodes protein.

A) True
B) False

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How alike are our genomes?


A) About 10%
B) About 25%
C) About 75%
D) Nearly 100%

E) C) and D)
F) None of the above

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The genotypes and phenotypes that result from a cross of AA and Aa (A = normal pigmentation and a = albinism) are


A) phenotypes:all normal; genotypes:50% homozygous dominant and 50% heterozygous.
B) phenotypes:50% normal and 50% albino; genotypes:all heterozygous.
C) phenotypes:75% normal and 25% albino; genotypes:75% heterozygous and 25% homozygous.
D) phenotypes:all albino; genotypes:50% heterozygous and 50% homozygous recessive.

E) A) and C)
F) B) and D)

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A

We can predict the likelihood of a particular inherited trait occurring in a particular family member by consulting the ways that genes are transmitted on chromosomes.

A) True
B) False

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After receiving a karyotype of a fetus, it is discovered that it has Klinefelter's syndrome. What does this designation indicate?


A) The fetus is female and resulted from one of the gametes having an extra X chromosome.
B) The fetus is an XY male.
C) The fetus is male and the result of a Y-bearing sperm fertilizing an XX egg.
D) The fetus is female and the result of only one gamete possessing an X chromosome.

E) A) and B)
F) B) and D)

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In genomic imprinting, the sex of a parent transmitting an allele is important in the phenotype of the offspring.

A) True
B) False

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