Huntington's disease is an autosomal dominant condition in humans. The disease is often not diagnosed until adulthood, sometimes after the person has had children (and possibly passed the Huntington's allele to their children). People with Huntington's disease are usually heterozygous and not homozygous dominant. ASsume that a person with Huntington's disease has a child with a person who does not have Huntington's disease. What is the probability that the child will have Huntington's disease? Support your answer with a Punnett square (on next page). 1
Huntington's disease is an autosomal dominant condition in humans. The disease is often not diagnosed until adulthood, sometimes after the person has had children (and possibly passed the Huntington's allele to their children). People with Huntington's disease are usually heterozygous and not homozygous dominant. ASsume that a person with Huntington's disease has a child with a person who does not have Huntington's disease. What is the probability that the child will have Huntington's disease? Support your answer with a Punnett square (on next page). 1
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
Publisher:Michael Cummings
Chapter11: Genome Alterations: Mutation And Epigenetics
Section: Chapter Questions
Problem 5QP: Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of...
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