Genetic Analysis: An Integrated Approach (2nd Edition)
2nd Edition
ISBN: 9780321948908
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Textbook Question
Chapter 3, Problem 20P
For each pedigree shown,
a. Identify which simple pattern of hereditary trans-mission (autosomal dominant, autosomal recessive, X-linked dominant, or X-linked recessive) is most likely to have occurred. Give genotypes for individuals involved in transmitting the trait.
b. Determine which other pattern(s) of transmission is/are possible. For each possible mode of transmission, specify the genotypes necessary for transmission to occur.
c. Identify which pattern(s) of transmission is/are impossible. Specify why transmission is impossible.
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Students have asked these similar questions
Ill.siven the following pedigree below, use Punnett squares for each of the following possibilities: a) X-
linked dominant, b) X-linked recessive, c) Autosomal dominant and d) Autosomal recessive in order
to determine what is the mode of transmission of this trait. Disease allele = Xª, x², A or a depending
on mode of transmission of the disease respectively. Unaffected X chromosome = X
*Homozygous unaffected/No
1
*2
carrier=Normal
II
1
*4
1
2 3
6.
7 8
a) X-linked dominant
11x12
b) X-linked recessive I 1 x1 2
c) Autosomal dominant 11x12
d) Autosomal recessive I1x12
IV.
Based on your analysis what is the mode of transmission for this disease?
O+
While studying of the family tree with history of hypertrichosis (hyper hirsutism of
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Select one:
a. Y-linked
b.
Autosomal-recessive
O c. Autosomal-dominant
d. Recessive, X-linked
e. Dominant, X-linked
A. For the following genotypes state the ABO blood phenotype.
JAJA
|B|O_
101⁰_
|A|B_
B. Using genetic diagrams, show how it is possible for a couple with a type A mother and a
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C. Using genetic diagrams show how a type AB person with a type O partner have offspring
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Chapter 3 Solutions
Genetic Analysis: An Integrated Approach (2nd Edition)
Ch. 3 - Examine the following diagrams of cells from an...Ch. 3 - Our closest primate relative, the chimpanzee, has...Ch. 3 -
3. In a test of his chromosome theory of...Ch. 3 - Cohesion between sister chromatids, as well as...Ch. 3 - 5. The diploid number of the hypothetical animal...Ch. 3 - 6. An organism has alleles R1 and R2 on one pair...Ch. 3 - Explain how the behavior of homologous chromosomes...Ch. 3 - 8. Suppose crossover occurs between the homologous...Ch. 3 -
9. Alleles A and a are on one pair of autosomes,...Ch. 3 - Prob. 10P
Ch. 3 - Describe the role of the following structures or...Ch. 3 - A womans father has ornithine transcarbamylase...Ch. 3 - In humans, hemophilia A (OMIM 306700) is an...Ch. 3 -
14. A wild-type male and a wild-type female...Ch. 3 - 15. A woman with severe discoloration of her tooth...Ch. 3 - 16. In a large metropolitan hospital, cells from...Ch. 3 - In cats, tortoiseshell coat color appears in...Ch. 3 - 18. The gene causing Coffin–Lowry syndrome (OMIM...Ch. 3 - 19. Four eye-color mutants in Drosophila—apricot,...Ch. 3 - 20. For each pedigree shown,
a. Identify which...Ch. 3 - 21. Use the blank pedigrees provided to depict...Ch. 3 - 22. Figure 3.22 (page 89) illustrates reciprocal...Ch. 3 - 23. In fruit flies, yellow body (y) is recessive...Ch. 3 - 24. In a species of fish, a black spot on the...Ch. 3 - LeschNyhan syndrome (OMIM 300322) is a rare...Ch. 3 - 26. In humans, SRY is located near a...Ch. 3 - 27. In an 1889 book titled Natural Inheritance...Ch. 3 - 30. Drosophila has a diploid chromosome number of...Ch. 3 - 29. A wild-type Drosophila male and female are...Ch. 3 - 28. In Drosophila, the X-linked echinus eye...Ch. 3 - 31. While examining a young tortoiseshell cat, you...Ch. 3 - 32. Redgreen color blindness in humans is...
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