HUMAN BIOLOGY (LOOSELEAF)-W/CONNECT
HUMAN BIOLOGY (LOOSELEAF)-W/CONNECT
16th Edition
ISBN: 9781260692174
Author: Mader
Publisher: MCG
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Chapter 21.1, Problem 3CYP
Summary Introduction

To summarize:

Three possible genotypes and their corresponding phenotypes.

Introduction:

There are two alleles for each trait. These alleles may be dominant or recessive depending on whether they are expressed or hidden in the trait. Dominant allele is designated by an upper case letter while recessive allele is designated by a lower case letter. For each trait we inherit one allele from each parent.

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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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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY