Genetic Analysis: An Integrated Approach (3rd Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
3rd Edition
ISBN: 9780134605173
Author: Mark F. Sanders, John L. Bowman
Publisher: PEARSON
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Chapter 5, Problem 14P

Nail–patella syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as the structure of kneecaps. The pedigree below shows the transmission of

nail–patella syndrome in a family along with ABO blood type.

Chapter 5, Problem 14P, 5.14 syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as

a. Is nail–patella syndrome a dominant or a recessivecondition? Explain your reasoning.

b. Does this family give evidence of genetic linkage between nail–patella syndrome and ABO blood group? Why or why not?

c. Using N and n to represent alleles at the nail–patella locus and I A, I B, and  i to represent ABO alleles, write thegenotypes of I-1 and I-2 as well as their five children in generation II .

d. Explain why III-6 has nail–patella syndrome and III-8 does not. Give genotypes for these two individuals.

e. Explain why III-11 has nail–patella syndrome and III-12 does not. Give genotypes for these two individuals.

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Sickle cell anemia is an inherited red blood cell disorder in which there are not enough healthy red blood cells to carry oxygen throughout the body. The allele that causes sickle-cell anemia is autosomal recessive (s), and the dominant allele can be represented by S. How many offspring will be affected by the disorder if the mother is a carrier, and the father appears to be normal? (Include the gender) a. b. How many will become carriers? (include the gender) A- 三三三 四 四 II !!
Below is a pedigree chart for a family that has a history of Alkaptonuria.   Individuals infected with this condition can have darkened skin, brown urine, and can suffer from joint damage and other complications.  Given this pedigree answer the following questions.   Given the data in the pedigree chart is this genetic condition autosomal dominant or autosomal recessive? What are the genotypes for #1, #2, and #3?  If either of the 4th generation "aa" females were to mate with a homozygous dominant male would any of their offspring illustrate the phenotype?  Why or why not?
a. On the basis of this pedigree, what is the most likely mode of inheritance for the disease? Explain your reasoning. b. Based your answer to part a, give the most likely genotypes for all family members in the pedigree.

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Genetic Analysis: An Integrated Approach (3rd Edition)

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