Genetics: Analysis and Principles
6th Edition
ISBN: 9781259616020
Author: Robert J. Brooker Professor Dr.
Publisher: McGraw-Hill Education
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Chapter 3, Problem 29CONQ
A woman with an abnormally long chromosome 13 (and a normal homolog of chromosome 13) has children with a man with an abnormally short chromosome 11 (and a normal homolog of chromosome 11). What is the probability of producing an offspring that will have both a long chromosome 13 and a short chromosome 11? If such a child is produced, what is the probability that this child will eventually pass both abnormal chromosomes to one of his or her offspring?
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Chapter 3 Solutions
Genetics: Analysis and Principles
Ch. 3.1 - 1. Which of the following is not found in a...Ch. 3.1 - When preparing a karyotype, which of the following...Ch. 3.1 - How many sets of chromosomes are found in a human...Ch. 3.2 - Binary fission a. is a form of asexual...Ch. 3.2 - Prob. 2COMQCh. 3.2 - What critical event occurs during the S phase of...Ch. 3.3 - 1. What is the function of the kinetochore during...Ch. 3.3 - Prob. 2COMQCh. 3.4 - Prob. 1COMQCh. 3.4 - Which phase of meiosis is depicted in the drawing...
Ch. 3.5 - In animals, a key difference between...Ch. 3.5 - Which of the following statements regarding plants...Ch. 3.6 - Which of the following is not one of the tenets of...Ch. 3.6 - A pea plant has the genotype TtRr. The independent...Ch. 3.6 - In mammals, sex is determined by a. the SRY gene...Ch. 3.6 - An abnormal fruit fly has two sets of autosomes...Ch. 3 - The process of binary fission begins with a single...Ch. 3 - 2. What is a homolog? With regard to genes and...Ch. 3 - What is a sister chromatid? Are sister chromatids...Ch. 3 - With regard to sister chromatids, which phase of...Ch. 3 - A species is diploid and has three chromosomes per...Ch. 3 - How does the attachment of kinetochore...Ch. 3 - 7. For the following events, specify whether they...Ch. 3 - Prob. 8CONQCh. 3 - A cell is diploid and contains three chromosomes...Ch. 3 - Prob. 10CONQCh. 3 - A eukaryotic cell is diploid and contains 10...Ch. 3 - Prob. 12CONQCh. 3 - 13. A cell has four pairs of chromosomes. Assuming...Ch. 3 - 14. With regard to question C13, how would the...Ch. 3 - Eukaryotic cells must sort their chromosomes...Ch. 3 - Why is it necessary for the chromosomes to...Ch. 3 - Nine-banded armadillos almost always give birth to...Ch. 3 - 18. A diploid species has four chromosomes per set...Ch. 3 - 19. Explain why the products of meiosis may not be...Ch. 3 - The period between meiosis I and meiosis II is...Ch. 3 - 21. List several ways in which telophase appears...Ch. 3 - Corn has 10 chromosomes per set, and the...Ch. 3 - The arctic fox has 50 chromosomes (25 per set),...Ch. 3 - 24. Let’s suppose that a gene affecting...Ch. 3 - 25. Describe the cellular differences between male...Ch. 3 - 26. At puberty, the testes contain a finite number...Ch. 3 - Describe the timing of meiosis I and II during...Ch. 3 - 28. Three genes (A, B, and C) are found on three...Ch. 3 - A woman with an abnormally long chromosome 13 (and...Ch. 3 - Assuming that such a fly would be viable, what...Ch. 3 - 31. What would be the sex of a human with each of...Ch. 3 - When studying living cells in a laboratory,...Ch. 3 - 2. In Morgan’s experiments, which result do you...Ch. 3 - 3. In his original studies of Figure 3.18, Morgan...Ch. 3 - How would you set up crosses to determine if a...Ch. 3 - 5. Occasionally during meiosis, a mistake can...Ch. 3 - Lets suppose that you have made a karyotype of a...Ch. 3 - Prob. 7EQCh. 3 - 8. White-eyed flies have a lower survival rate...Ch. 3 - A rare form of dwarfism that also included hearing...Ch. 3 - 10. Discuss why crosses (i.e., the experiments of...Ch. 3 - Prob. 11EQCh. 3 - 12. Experimentally, how do you think researchers...Ch. 3 - 1. In Figure 3.18, Morgan obtained a white-eyed...Ch. 3 - 3. Discuss the principles of the chromosome theory...
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- Two phenotypically normal parents produce a phenotypicallyabnormal child in which chromosome 5 is missing part of its longarm but has a piece of chromosome 7 attached to it. The child alsohas one normal copy of chromosome 5 and two normal copies ofchromosome 7. With regard to chromosomes 5 and 7, what do youthink are the chromosomal compositions of the parents?arrow_forwardTwo phenotypically normal parents produce an abnormal son in which chromosome 14 is missing part of its short arm but has a piece of chromosome 21 attached to it. The child also has one normal copy of chromosome 14 and two normal copies of chromosome 21. (i) With regard to chromosome 14 and 21, what do you think are the chromosomal compositions of the parent? (ii) Draw the pairing of the translocated chromosomes in the parent during meiosis and name the segregation pattern that contributes to the abnormal karyotype. (iii) State the syndrome and write the notation for this child's karyotype.arrow_forwardTwo phenotypically normal parents produce a phenotypically abnormal child in which chromosome 5 is missing part of its long arm but has a piece of chromosome 7 attached to it. The child also has one normal copy of chromosome 5 and two normal copies of chromosome 7. With regard to chromosomes 5 and 7, what do you think are the chromosomal compositions of the parents? Would it most likely be reciprocal translocation? It wouldn't be simple translocation because then the child would have the entirety of one chromosome and only some of the other, but in this case, there is only partial chromosome 5 and chromosome 7?arrow_forward
- A 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_forwardA woman with an abnormally long chromosome 13 (and a normalhomolog of chromosome 13) has children with a man with anabnormally short chromosome 11 (and a normal homolog of chromosome 11). What is the probability of producing an offspringthat will have both a long chromosome 13 and a short chromosome11? If such a child is produced, what is the probability that thischild will eventually pass both abnormal chromosomes to one ofhis or her offspring?arrow_forwardA boy with Klinefelter syndrome (47,XXY) is born to a mother who is phenotypically normal and a father who has the X- linked skin condition called anhidrotic ectodermal dysplasia. The boy has patches of normal skin and patches of abnormal skin. Which of the following statemnets likely explains these observations? The father contributed the extra X chromosome in the son as a result of a non-disjunction in meiosis I during spermatogenesis. The mother contributed the extra X chromosome in the son as a result of a non-disjunction in meiosis II during oogenesis. The mother contributed the extra X chromosome in the son as a result of a non-disjunction in meiosis I during oogenesis. The father contributed the extra X chromosome in the son as a result of a non-disjunction in meiosis II during spermatogenesis. Either parent could have contributed to the extra X chromosome in the son as a results of disjunction in either meiosis I or meiosis II during…arrow_forward
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