Exam 7: Sex Determination and Sex Chromosomes
Exam 1: Introduction to Genetics44 Questions
Exam 2: Mitosis and Meiosis51 Questions
Exam 3: Mendelian Genetics63 Questions
Exam 4: Extensions of Mendelian Genetics66 Questions
Exam 5: Chromosome Mapping in Eukaryotes43 Questions
Exam 6: Genetic Analysis and Mapping in Bacteria and Bacteriophages50 Questions
Exam 7: Sex Determination and Sex Chromosomes47 Questions
Exam 8: Chromosome Mutations: Variation in Number and Arrangement47 Questions
Exam 9: Extranuclear Inheritance37 Questions
Exam 10: DNA Structure and Analysis50 Questions
Exam 11: DNA Replication and Recombination50 Questions
Exam 12: DNA Organization in Chromosomes34 Questions
Exam 13: The Genetic Code and Transcription51 Questions
Exam 14: Translation and Proteins50 Questions
Exam 15: Gene Mutation, Dna Repair, and Transposition53 Questions
Exam 16: Regulation of Gene Expression in Prokaryotes41 Questions
Exam 17: Regulation of Gene Expression in Eukaryotes43 Questions
Exam 18: Developmental Genetics41 Questions
Exam 19: Cancer and Regulation of the Cell Cycle48 Questions
Exam 20: Recombinant Dna Technology54 Questions
Exam 21: Genomics, Bioinformatics, and Proteomics44 Questions
Exam 22: Applications and Ethics of Genetic Engineering and Biotechnology36 Questions
Exam 23: Quantitative Genetics and Multifactorial Traits52 Questions
Exam 24: Neurogenetics29 Questions
Exam 25: Population and Evolutionary Genetics58 Questions
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Although triple-X human females typically have normal offspring, what kinds of gametes, with respect to the X chromosomes, would you expect from such XXX females? Draw meiotic stages that show the gametes that are expected to be produced.
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Correct Answer:
One form of hemophilia is caused by a sex-linked recessive gene. Assume that a man with hemophilia marries a phenotypically normal woman whose father had hemophilia. What is the probability that they will have a daughter with hemophilia? (Note: In this problem, you must include the probability of having a daughter in your computation of the final probability.)
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(Multiple Choice)
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Correct Answer:
C
An individual with Klinefelter syndrome generally has one Barr body.
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(True/False)
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Correct Answer:
True
Data produced by C. Bridges in the early part of this century indicate that sex in Drosophila is determined by ________.
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The sex of birds, some insects, and other organisms is determined by a ZW chromosomal arrangement in which the males have like sex chromosomes (ZZ) and females are ZW (similar to XY in humans). Assume that a recessive lethal allele on the Z chromosome causes death of an embryo in birds. What sex ratio would result in the offspring if a cross were made between a male heterozygous for the lethal allele and a normal female?
(Multiple Choice)
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Glucose-6-phosphate dehydrogenase (G6PD) deficiency is inherited as an X-linked recessive gene in humans. A woman whose father suffered from G6PD marries a normal man.
a) What proportion of their sons is expected to be G6PD?
b) If the husband were not normal, but were G6PD deficient, would you change your answer in part (a)?
(Short Answer)
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Assume that a man who carries an X-linked gene has children. Assuming normal meiosis and random combination of gametes, the man would pass this gene to ________.
(Multiple Choice)
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Give the sex-chromosome constitution (X and Y chromosomes) and possible genotypes of offspring resulting from a cross between a white-eyed female (Xw XwY) and a wild-type male (normal chromosome complement) in Drosophila melanogaster. Include all zygotic combinations whether viable or inviable.
(Essay)
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In Drosophila, the sex of a fly with the karyotype XO:2A is ________.
(Short Answer)
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Normally in humans, all the sons of a male showing a sex-linked phenotype will inherit the trait.
(True/False)
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Assume that you are told that a particular organism, Drosophila, has the XO chromosome complement. You are also told that the autosomal complement is a normal 2n. You know that in humans the XO complement is female determining. Would you be correct in assuming that the Drosophila sex for XO is also female? Choose the answer that includes the correct explanation.
(Multiple Choice)
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A color-blind woman with Turner syndrome (XO) has a father who is color blind.
Given that the gene for the color-blind condition is recessive and X-linked, provide a likely explanation for the origin of the color-blind and cytogenetic conditions in the woman.
(Essay)
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Klinefelter and Turner syndromes have how many chromosomes, respectively?
(Short Answer)
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In Drosophila, an individual female fly was observed to be of the XXY chromosome complement (normal autosomal complement) and to have white eyes as contrasted with the normal red eye color of wild type. The female's father had red eyes, and the mother had white eyes. Knowing that white eyes are X-linked and recessive, present an explanation for the genetic and chromosomal constitution of the XXY, white-eyed individual. It is important that you state in which parent and at what stage the chromosomal event occurred that caused the genetic and cytogenetic abnormality.
(Essay)
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In Drosophila, sex is determined by a balance between the number of haploid sets of autosomes and the number of ________.
(Multiple Choice)
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Under what condition might a human female have the XY sex chromosome complement?
(Essay)
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For an individual with the XXY chromosomal composition, the expected number of Barr bodies in interphase cells is ________.
(Multiple Choice)
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