Laboratory Manual for Anatomy and Physiology, 6e Loose-Leaf Print Companion
Laboratory Manual for Anatomy and Physiology, 6e Loose-Leaf Print Companion
6th Edition
ISBN: 9781119304142
Author: Connie Allen, Valerie Harper
Publisher: WILEY
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Chapter 41, Problem 2MCI
Summary Introduction

To determine: The percentages of each genotype and phenotype of the children produced by the mother with sickle-cell anemia and a father with the sickle-cell trait from the Punnett square.

Introduction: Sickle cell anemia is an inherited disorder of hemoglobin in the red blood cells (RBC). The abnormal hemoglobin causes the distorted (sickled) or irregular appearance of the red blood cell. These sickle-shaped red blood cells have a short life span and also cause various problems in circulation.

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*Example 2: Tracing the path of an autosomal dominant trait Trait: Neurofibromatosis Forms of the trait: The dominant form is neurofibromatosis, caused by the production of an abnormal form of the protein neurofibromin. Affected individuals show spots of abnormal skin pigmentation and non-cancerous tumors that can interfere with the nervous system and cause blindness. Some tumors can convert to a cancerous form. i The recessive form is a normal protein - in other words, no neurofibromatosis.moovi A typical pedigree for a family that carries neurofibromatosis is shown below. Note that carriers are not indicated with half-colored shapes in this chart. Use the letter "N" to indicate the dominant neurofibromatosis allele, and the letter "n" for the normal allele. Nn nn nn 2 nn Nn A 3 N-
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Chapter 41 Solutions

Laboratory Manual for Anatomy and Physiology, 6e Loose-Leaf Print Companion

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