Concepts of Genetics (12th Edition)
12th Edition
ISBN: 9780134604718
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino, Darrell Killian
Publisher: PEARSON
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Textbook Question
Chapter 7, Problem 16PDQ
Indicate the expected number of Barr bodies in interphase cells of individuals with Klinefelter syndrome; Turner syndrome; and karyotypes 47,XYY, 47,XXX, and 48,XXXX.
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Indicate the expected number of Barr bodies in interphase cells of individuals with Klinefelter syndrome; Turner syndrome; and karyotypes 47,XYY, 47,XXX, and 48,XXXX.
Assuming no other abnormalities, classify each of the following human sex chromosome complements as to whether or not individuals with that complement will be morphologically male or female. Three human sex chromosome complements will be classified as male and three will be classified as female.
XXY
XYY
XXX
XO
XY
XX
For an individual with the XXXYY chromosomal composition, the expected number of Barr bodies in interphase cells is ________.
one
variable
zero
three
two
Chapter 7 Solutions
Concepts of Genetics (12th Edition)
Ch. 7 - Campomelic dysplasia (CMD1) is a congenital human...Ch. 7 - Carbon Copy (CC), the first car produced from a...Ch. 7 - Gender is someones conscious and unconscious...Ch. 7 - Gender is someones conscious and unconscious...Ch. 7 - HOW DO WE KNOW? In this chapter, we have focused...Ch. 7 - Review the Chapter Concepts list on p. 151. These...Ch. 7 - Distinguish between the concepts of sexual...Ch. 7 - Contrast the XX/XY and XX/X0 modes of sex...Ch. 7 - Describe the major difference between sex...Ch. 7 - How do mammals, including humans, solve the dosage...
Ch. 7 - The phenotype of an early-stage human embryo is...Ch. 7 - What specific observations (evidence) support the...Ch. 7 - Describe how nondisjunction in human female...Ch. 7 - An insect species is discovered in which the...Ch. 7 - When cows have twin calves of unlike sex...Ch. 7 - An attached-X female fly, XXY (see the Insights...Ch. 7 - Assume that on rare occasions the attached X...Ch. 7 - It has been suggested that any male-determining...Ch. 7 - What is a Barr body, and where is it found in a...Ch. 7 - Indicate the expected number of Barr bodies in...Ch. 7 - Define the Lyon hypothesis.Ch. 7 - Can the Lyon hypothesis be tested in a human...Ch. 7 - Predict the potential effect of the Lyon...Ch. 7 - Cat breeders are aware that kittens expressing the...Ch. 7 - In mice, the Sry gene (see Section 7.2) is located...Ch. 7 - The genes encoding the red-and...Ch. 7 - What is the role of the enzyme aromatase in sexual...Ch. 7 - In the wasp Bracon hebetor, a form of...Ch. 7 - The Amami spiny rat (Tokudaia osimensis) lacks a Y...Ch. 7 - In mice, the X-linked dominant mutation Testicular...Ch. 7 - When the cloned cat Carbon Copy (CC) was born (see...Ch. 7 - In reptiles, sex determination was thought to be...Ch. 7 - In chickens, a key gene involved in sex...
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- Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?arrow_forwardGive the typical sex-chromosome complement found in the cells of people with Turner syndrome, with Klinefelter syndrome, and with androgen-insensitivity syndrome. What is the sex-chromosome complement of triple-X females?arrow_forwardFor the following chromosome complements, what is the phenotypic sex of a person who has Q. XO with a copy of the SRY gene on an autosomal chromosome?arrow_forward
- How many Barr bodies are contained within the nucleus of a person with Monosomy X? In thenucleus of a person with Trisomy X? A person with XYY syndrome? Please explain.arrow_forwardExplain why a person with Klinefelter Syndrome (XXY) still exhibits abnormal phenotypes despite the fact that one of the extra X Chromosome is inactivated practically leaving an XY active sex chromosomes similar to a normal male?arrow_forwardThe Xg cell-surface antigen is coded for by a gene located on the X chromosome. No equivalent gene exists on the Y chromosome. Two codominant alleles of this gene have been identified: Xg1 and Xg2. A woman of genotype Xg2/Xg2 bears children with a man of genotype Xg1/Y, and they produce a son with Klinefelter syndrome of genotype Xg1/Xg2Y. Using proper genetic terminology, briefly explain how this individual was generated. In which parent and in which meiotic division did the mistake occur?arrow_forward
- A color-blind, chromatin-positive male child (one Barr body) has a maternal grandfather who was color blind. The boy’s mother and father are phenotypically normal. Construct and support (using appropriately labeled diagrams) a rationale whereby the chromosomal and genetic attributes of the chromatin-positive male are fully explained.arrow_forwardDraw a family pedigree to describe the mode of inheritance of G6PD deficiency, Hemophilia, Erbs Duchene musculo-dysrophy and neurofibromatosisarrow_forwardFor the following chromosome complements, what is the phenotypic sex of a person who has Q. XXYY with one copy of the SRY gene deleted?arrow_forward
- A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown?arrow_forwardA man with blood type O (genotype ii) has a father with blood type A and a mother with blood type B. Is this man a legitimate child of these parents? What is a possible phenotype of an individual that results from a woman with type AB blood and a man with type B blood? Explain with diagrams.arrow_forwardGive several examples of chromosome number disorders.arrow_forward
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