Human Heredity: Principles and Issues (MindTap Course List)
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN: 9781305251052
Author: Michael Cummings
Publisher: Cengage Learning
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Chapter 4, Problem 13QP

Analysis of Autosomal Recessive and Dominant Traits

The father of 12 children begins to show symptoms of Huntington disease.

  1. a. What is the probability that Sam, the man’s second-oldest son (II-2), will suffer from the disease if he lives a normal life span? (Sam’s mother and her ancestors do not have the disease.)
  2. b. Can you infer anything about the presence of the disease in Sam’s paternal grandparents?
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Pedigree 2: A. What is the most likely mode of inheritance of this disease? Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive. B State the genotypes of individuals # 1 #4. C If individual #3 has another daughter with the same partner, what is the probability that this daughter will be affected (show the disease)?
Consider the following pedigree. 하 3 10 (5 3 2 (a) What pattern of transmission is most consistent with this pedigree? (1) autosomal recessive, (2) autosomal dominant, (3) X-linked recessive, (4) X-linked dominant. (b) If individual V-2 marries a normal individual, and if the condition has a pene-trance of 85 percent, what is the probability that their second child will express the trait? (c) On the third line, what does the diamond with a 10 in the middle mean?
MENDELIAN MODE OF INHERITANCE AND PEDIGREE ANALYSIS 1. Dent disease is a rare disorder of the kidney in which there is impaired reabsorption of filtered solutes and progressive renal failure. The following pedigree shows the pattern of inheritance for this disorder. a. On the basis of this pedigree, what is the most likely mode of inheritance for the disease? b. From your answer to part a, give the most likely genotypes for the following persons in the pedigree: 1-1: 1-2: Il-5: Il-8: III-1: III-3: IV-2: IV-1:

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Human Heredity: Principles and Issues (MindTap Course List)

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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY