Essentials of Genetics (9th Edition) - Standalone book
9th Edition
ISBN: 9780134047799
Author: William S. Klug, Michael R. Cummings, Charlotte A. Spencer, Michael A. Palladino
Publisher: PEARSON
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Chapter 6, Problem 26PDQ
A normal female is discovered with 45 chromosomes, one of which exhibits a Robertsonian translocation containing most of chromosomes 18 and 21. Discuss the possible outcomes in her offspring when her husband contains a normal karyotype.
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A normal female is discovered with 45 chromosomes, one of which exhibits a Robertsonian translocation containing most of chromosomes 15 and 21. Discuss the possible outcomes in her offspring when her husband contains a normal karyotype.
An individual heterozygous for a reciprocal translocation possesses the following chromosomes:
A B • C D E F G
A B • C D V W X
R S • T U E F G
R S • T U V W X
Q. Draw the pairing arrangement of these chromosomes in prophase I of meiosis.
A human female with Turner syndrome (45,X) also
expresses the X-linked trait hemophilia, as did her father.
Which of her parents underwent nondisjunction during meiosis, giving rise to the
gamete responsible for the syndrome?
Chapter 6 Solutions
Essentials of Genetics (9th Edition) - Standalone book
Ch. 6 - CASE STUDY| Fish tales Aquatic vegetation...Ch. 6 - CASE STUDY |Fish tales Aquatic vegetation...Ch. 6 - CASE STUDY |Fish tales
Aquatic vegetation...Ch. 6 - HOW DO WE KNOW? In this chapter, we focused on...Ch. 6 -
CONCEPT QUESTION
2. Review the Chapter Concepts...Ch. 6 -
3. Define these pairs of terms, and distinguish...Ch. 6 -
4. For a species with a diploid number of 18,...Ch. 6 - What explanation has been proposed to explain why...Ch. 6 - Contrast the fertility of an allotetraploid with...Ch. 6 -
7. Why do human monosomies most often fail to...
Ch. 6 -
8. Describe the origin of cultivated American...Ch. 6 - Predict how the synaptic configurations of...Ch. 6 - Inversions are said to “suppress crossing over.”...Ch. 6 -
11. Predict the genetic composition of gametes...Ch. 6 - Human adult hemoglobin is a tetramer containing...Ch. 6 -
13. The primrose, Primula kewensis, has 36...Ch. 6 - Certain varieties of chrysanthemums contain 18,...Ch. 6 - Drosophila may be monosomic for chromosome 4, yet...Ch. 6 - Mendelian ratios are modified in crosses involving...Ch. 6 -
17. Having correctly established the F2 ratio in...Ch. 6 -
18. In a cross between two varieties of corn,...Ch. 6 -
19. A couple planning their family are aware that...Ch. 6 -
20. A woman who sought genetic counseling is...Ch. 6 - The woman in Problem 20 has had two miscarriages....Ch. 6 -
22. In a recent cytogenetic study on 1021 cases...Ch. 6 -
23. A boy with Klinefelter syndrome (47,XXY) is...Ch. 6 - In a human genetic study, a family with five...Ch. 6 - A 3-year-old child exhibited some early indication...Ch. 6 - A normal female is discovered with 45 chromosomes,...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- Human sex chromosomes are XX for females and XY for males. a. With respect to an X-linked gene, how many different types of gametes can a male produce? b. If a female is homozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele? c. If a female is heterozygous for an X-linked allele, how many different types of gametes can she produce with respect to this allele?arrow_forwardGiven the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?arrow_forwardA misaligned crossover between two homologous chromosomes usually results in:arrow_forward
- A woman with no phenotype is known to have a 14:21 translocation. Please answer questions 1 and 2. 1. With respect to only chromosomes 14 and 21, how many distinct chromosome combinations will happen in her eggs? What portion will be viable? 2. If she has children with a normal man (no translocations), what is the probability that they have a daughter with Down Syndrome or a son with no phenotype?arrow_forwardA diploid (2n) trihybrid individual with the genotype EeFfGg can make eight genetically different gametes. Loci E/e and F/f are on chromosome 1 and locus G/g is on chromosome 2. Explain how a gamete containing the alleles e, f and g may be produced by meiosis. Refer specifically to meiotic events occurring during Prophase I, Metaphase I, Anaphase I and Anaphase II. (NB: remember to refer to the organism above).arrow_forwardA human female with Turner syndrome (45,X) alsoexpresses the X-linked trait hemophilia, as did her father.Which of her parents underwent nondisjunction during meiosis,giving rise to the gamete responsible for the syndrome?arrow_forward
- 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 XXarrow_forwardAn individual is heterozygous for a reciprocal translocation, with the following chromosomes: A • B C D E F A • B C V W X R ST • U D E F R ST • U V W X Q. Draw a picture of these chromosomes pairing in prophase I of meiosis.arrow_forwardAn individual heterozygous for a reciprocal translocation possesses the following chromosomes: A B • C D E F G A B • C D V W X R S • T U E F G R S • T U V W X Q. Diagram the alternate, adjacent-1, and adjacent-2 segregation patterns in anaphase I of meiosis.arrow_forward
- If the proband (III-2) marries a carrier woman, what is the probability that they will have an affected son? affected daughter? (Please show complete solution. Thanks.)arrow_forwardA couple comes into a fertility clinic. A chromosome preparation is made for each and the male is found to have an aberrant karyotype. He is heterozygous for two sets of reciprocal translocations involving four different chromosome pairs. What proportion of his gametes are expected to be functional and viable?arrow_forwardA phenotypically normal individual has the following combinations of normal and abnormal chromosomes:The normal chromosomes are shown on the left in each pair.Suggest a series of events (breaks, translocations, crossovers, etc.)that may have produced this combination of chromosomes.arrow_forward
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