Campbell Biology
Campbell Biology
12th Edition
ISBN: 9780135188743
Author: Urry
Publisher: PEARSON
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Chapter 14.4, Problem 1CC
Summary Introduction

To know: The probability for two genetic crosses in the given case.

Introduction: Cystic fibrosis is a disease that is caused due to defective genes. It is a recessive disorder that is passed on to children by their parents. It can affect the lungs, pancreas, and digestive system. It is caused when both parents are carrying one recessive gene and children must inherit both genes in order to get affected.

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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 14 Solutions

Campbell Biology

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