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 !!
Please consider the following pedigree. Assume that people who marry in to the family do not carry the allele unless otherwise indicated. Assume complete penetrance. image attached   a. Is it possible for the inheritance pattern for the trait illustrated in this pedigree to be as a result of each of the following? Answer yes or no.  (i) an autosomal recessive allele (AR)(ii) an autosomal dominant allele (AD)(iii) a X-linked recessive allele (XR)(iv) a X-linked dominant allele (XD) b. Provide a set of parents that definitively supports your answers in (a).
Brachydactyly type D is human autosomal dominant condition in which the thumbs are abnormally short and broad. In most cases, both thumbs are affected, but occasionally just one thumb is involved. The pedigree above shows a family in which brachydactlyly type D is segregating. Filled circles and squares represent females and males who have involvement of both thumbs. Half-filled in symbols represent family members with just one thumb affected?  (Picture attached) There is evidence of variable expressivity and incomplete penetrance in this family. Which individual is most likely nonpenetrant for the trait?   A) III-11 B) IV-1 C) IV-5 D) III-10 E) II-4

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Genetic Analysis: An Integrated Approach (3rd Edition)

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