A) It initiates the X inactivation process in females.
B) It is located on the X chromosome and causes the X to pair with the Y chromosome during male meiosis.
C) It is located on the Y chromosome and initiates the developmental pathway toward the male phenotype.
D) It is located on an autosomal chromosome and represses expression of autosomal genes in order to balance their expression level with genes on the X chromosome.
E) None of the answers is correct.
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Multiple Choice
A) 0
B) 1/8
C) 1/4
D) 1/2
E) 3/4
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Multiple Choice
A) Dominance
B) Discontinuous characteristic
C) Polygenic characteristic
D) Phenocopy
E) Pleiotropy
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Multiple Choice
A) gene on the X chromosome that is responsible for female development.
B) patch of cells that has a phenotype different from surrounding cells because of variable X inactivation.
C) inactivated X chromosome, visible in the nucleus of a cell that is normally from a female mammal.
D) extra X chromosome in a cell that is the result of nondisjunction.
E) extra Y chromosome in a cell that is the result of nondisjunction.
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Multiple Choice
A) 0%
B) 100%
C) 75%
D) 50%
E) 25%
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Multiple Choice
A) Recessive epistasis
B) Dominant epistasis
C) Complementation
D) Mutation
E) Suppression
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Multiple Choice
A) XO women do not have a copy of the SRY gene.
B) Some genes remain active on the inactive X chromosome, and XX women will have two copies of these genes expressed while XO women only have one copy expressed.
C) In XO women, the single X chromosome has no partner to pair with during mitosis so that each cell division is delayed by pairing problems with the single X not finding a pairing partner.
D) XO women have two copies of the SRY gene so that they are forced to develop partway along the male pathway during embryogenesis.
E) None of these are reasonable explanations.
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Multiple Choice
A) rr PP × rr pp
B) RR Pp × rr pp
C) Rr PP × rr pp
D) Rr Pp × rr pp
E) rr Pp × rr pp
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Multiple Choice
A) B/bg
B) Br/bg
C) br/by
D) by/bg
E) B/by
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Multiple Choice
A) bb WW
B) bb Ww
C) Bb Ww
D) Bb ww
E) BB ww
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Multiple Choice
A) Some women had only one X chromosome, and it is inactive.
B) Some women had three copies of the X chromosome which allowed them to make extra amounts of gene products for their X-linked genes.
C) The women with normal clotting times probably had a mother with hemophilia while those with abnormal clotting times probably had fathers with hemophilia.
D) Random X inactivation probably results in individuals with different proportions of cells in their bodies expressing the normal allele at the hemophilia locus.
E) In women with abnormal clotting times, there was probably an epistatic interaction between an allele on the X chromosome and an allele on an autosomal gene that reduced the expression of the X-linked gene.
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Multiple Choice
A) female offspring have one X chromosome, and it is inherited from their father.
B) male offspring have one X chromosome, and it is inherited from their mother.
C) male offspring have one X chromosome, and it is inherited from their father.
D) female offspring have one X chromosome, and it is inherited from their mother.
E) None of the statements is true.
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Multiple Choice
A) homogametic; heterogametic
B) pleiotropic: epistatic
C) heterogametic; homogametic
D) epistatic; pleiotropic
E) epistatic; heterogametic
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Multiple Choice
A) A
B) B
C) O
D) AB
E) Any of the above is a possible blood type of the father.
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Multiple Choice
A) X-linked inheritance
B) Evolution of the Y chromosome
C) Dosage compensation between males and females
D) Development of male and female secondary sexual characteristics
E) Sex determination
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Essay
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View Answer
Multiple Choice
A) XXY
B) XXXY
C) XXXXY
D) All of the answers are correct.
E) None of the answers is correct.
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Essay
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View Answer
Multiple Choice
A) A_ B_
B) AA Bb
C) aa B_
D) aa bb
E) A_ B_ and A_ bb
Correct Answer
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Multiple Choice
A) 0
B) 1
C) 2
D) 3
E) 4
Correct Answer
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