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Questions

Question 1

In humans and other mammals, what term is used to describe females who typically have two X chromosomes?

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Question 2

What is the primary genetic trigger for the development of testes in the early human embryo?

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Question 3

What are the regions at the ends of the X and Y chromosomes that contain homologous sequences and allow for pairing during meiosis called?

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Question 4

In the human sex differentiation pathway, the SRY protein, a transcription factor, directly activates the expression of which other key gene?

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Question 5

An individual with an XX genotype has the SRY gene translocated to one of their X chromosomes. What is the most likely anatomical phenotype for this individual?

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Question 6

What is the chromosomal basis for Swyer syndrome?

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Question 7

What mechanism of dosage compensation is used in the fruit fly, Drosophila melanogaster?

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Question 8

The patchwork fur color of calico and tortoiseshell cats is a striking visual example of what genetic phenomenon?

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Question 9

What is the most likely karyotype for a rare male calico cat?

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Question 10

What term refers to a person's innate, deeply felt sense of being a girl, boy, a blend of both, or an alternative identity?

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Question 11

According to the text, Complete Androgen Insensitivity (CAIS) is caused by mutations in which type of gene?

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Question 12

In the case of red-green colorblindness in humans, why can a female heterozygous for a recessive colorblindness allele usually see color normally?

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Question 13

What is the defining characteristic of a sex-limited trait?

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Question 14

In a cross between a red-eyed heterozygous female fruit fly (Xw+/Xw-) and a white-eyed male (Xw-/Y), what proportion of the female offspring is expected to have white eyes?

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Question 15

Why are autosomal aneuploidies generally more severe and less common in the human population than sex chromosome aneuploidies?

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Question 16

What is the key difference between sex-determination genes and sex-linked genes?

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Question 17

A condition in which XY individuals have a loss of function mutation in the enzyme that converts testosterone to dihydrotestosterone (DHT), often resulting in ambiguous external genitalia at birth, is known as what?

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Question 18

The visually observable structure in the nucleus of a mammalian female cell that represents the condensed, inactive X chromosome is called what?

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Question 19

What hormone, produced by the developing testes, causes the degeneration of the Müllerian duct in a developing human male embryo?

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Question 20

In a reciprocal cross experiment with Drosophila, a white-eyed female is crossed with a red-eyed (wild-type) male. What are the expected phenotypes of the F1 generation?

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Question 21

A human individual with a single X chromosome and no second sex chromosome (XO) has which condition?

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Question 22

What is the chromosomal system of sex determination in birds?

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Question 23

The development of female structures like the uterus and oviducts from the Müllerian duct is triggered by which hormone?

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Question 24

According to some estimates including atypical ploidy, approximately what percentage of the human population has a Difference of Sex Development (DSD)?

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Question 25

Why are individuals with chromosomal aneuploidies like XXY and XXX generally viable and often have few phenotypic effects?

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Question 26

What is the primary factor that determines sex in honeybees?

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Question 27

What is a cisgender individual?

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Question 28

Approximately how many genes are carried on the human X chromosome?

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Question 29

In birds with a ZW sex-determination system, the DMRT1 gene on the Z chromosome is haploinsufficient. What does this mean for ZW individuals?

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Question 30

Which condition results from mutations in the enzyme 21-hydroxylase, leading to a buildup of testosterone and masculinization of external genitalia in XX individuals?

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Question 31

Why do traits that follow standard Mendelian patterns of inheritance show no difference in reciprocal crosses, while sex-linked traits often do?

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Question 32

In mammals, which long non-coding RNA molecule is responsible for coating the X chromosome to be inactivated and initiating the silencing process?

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Question 33

In the absence of SRY, an alternative set of molecular signals, including WNT4 and RSPO1, leads to the development of what structures?

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Question 34

What is the key functional difference between a sex-influenced trait and a sex-linked trait?

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Question 35

In the case of Hemophilia A, a recessive X-linked disorder, why do heterozygous females typically not have the disease?

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Question 36

A person with an XYY genotype would be best described as having which condition?

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Question 37

What is the definition of anatomical sex?

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Question 38

The work of Thomas Hunt Morgan with the white-eyed fruit fly was crucial for demonstrating what fundamental concept?

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Question 39

In the cross of a red-eyed heterozygous female fruit fly (Xw+/Xw-) and a red-eyed male (Xw+/Y), what percentage of the male offspring will have white eyes?

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Question 40

Skewed X-inactivation, where one X chromosome is inactivated in significantly more than 50 percent of cells, can lead to what outcome in a female heterozygous for a recessive X-linked disorder?

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Question 41

What is the primary characteristic of a Y-linked trait's inheritance pattern?

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Question 42

Which part of the early human embryo develops into the male reproductive tract under the influence of testosterone?

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Question 43

The red and green cone pigment genes, which are crucial for color vision, are located on which chromosome in humans?

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Question 44

Which of these is NOT an example of a Difference of Sex Development (DSD) mentioned in the text?

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Question 45

In the mechanism of dosage compensation in C. elegans, what happens to the X chromosomes in XX individuals?

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Question 46

Why do chromosomal males (XY) always express the phenotype determined by their one allele for an X-linked gene?

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Question 47

In the context of the genetics of sex, the term 'intersex' is another term for what?

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Question 48

What is the consequence of a loss of function in the Wolffian duct system in a developing embryo?

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Question 49

In the ABO blood type system described in the text, the O allele is recessive. If a tortoiseshell female cat (X^O X^B) has blood type O (genotype ii), and she mates with an orange male cat (X^O Y) who has blood type AB (genotype I^A I^B), what is the probability of them having an orange, male kitten with blood type A?

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Question 50

A diploid individual can only have two alleles for a given gene, but in a biological population, there may be many different variations. The text describes this in the context of the ABO blood group and the O gene in cats. What concept does this illustrate?

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