Campbell Essential Biology with Physiology (6th Edition)
Campbell Essential Biology with Physiology (6th Edition)
6th Edition
ISBN: 9780134711751
Author: Eric J. Simon, Jean L. Dickey, Jane B. Reece
Publisher: PEARSON
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Chapter 9, Problem 3SQ
Summary Introduction

Introduction: Edward was found to be heterozygous (Ss) for the sickle-cell trait. In this disease the effect of a single gene on a chromosome is amplified. It affects many genes coding for sickle cell anemia. The shape of the red blood cells changes and they become crescent shaped. They ability to bind to oxygen decreases in blood. The dominant gene for sickle cell anemia in the genotype is represented by S and the recessive gene in the genotype is represented by s. The depiction for hemoglobin is depicted by Hb and in a cross it can be depicted as HbS for the dominant gene and Hbs for the recessive gene.

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Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is referred to as a sex-linked disease. The recessive allele causes the disease. A man with hemophilia (xhy) marries a woman who is homozygous dominant (XHXH. A. Illustrate using a Punnett square the probability that their children will have the disease. B. Will any of their children have the disease? C. Predict the probabilities of their children having the disease.
Hemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait, what is the chance of having children who are hemophiliacs? (XH = normal; Xh= hemophiliac) *       a. 0%   b. 75%   c. 100%   d. 25%
Edward was found to be heterozygous (Ss) for the sickle-cell trait. The alleles represented by the letters S and s are a. on the X and Y chromosomes. b. linked. c. on homologous chromosomes. d. both present in each of Edward’s sperm cells.
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