Mutations in the genes for clotting factor VIII and IX cause hemophilia A and B, respectively. A woman may be heterozygous for mutations in both genes, with a mutated factor VIII allele on one X chromosome, and a mutated factor IX allele on the other. All of her sons should have either hemophilia A or B. However, on rare occasions, one of these women gives birth to a son who does not have hemophilia, and his one X chromosome does not have either mutated allele. Explain. | StudySoup

Textbook Solutions for Biology: The Unity and Diversity of Life

Chapter 14 Problem 9

Question

Mutations in the genes for clotting factor VIII and IX cause hemophilia A and B, respectively. A woman may be heterozygous for mutations in both genes, with a mutated factor VIII allele on one X chromosome, and a mutated factor IX allele on the other. All of her sons should have either hemophilia A or B. However, on rare occasions, one of these women gives birth to a son who does not have hemophilia, and his one X chromosome does not have either mutated allele. Explain.

Solution

Step 1 of 3

Mutations in the genes for clotting factor VIII and IX cause hemophilia A and B, respectively. A woman can be heterozygous for mutations in both genes, meaning she carries a mutated factor VIII allele on one X chromosome and a mutated factor IX allele on the other.

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Title Biology: The Unity and Diversity of Life 15 
Author Cecie Starr , Ralph Taggart , Christine Evers , Lisa Starr
ISBN 9781337408332

Mutations in the genes for clotting factor VIII and IX cause hemophilia A and B, respectively. A woman may be heterozygous for mutations in both genes, with a mutated factor VIII allele on one X chromosome, and a mutated factor IX allele on the other. All of her sons should have either hemophilia A or B. However, on rare occasions, one of these women gives birth to a son who does not have hemophilia, and his one X chromosome does not have either mutated allele. Explain.

Chapter 14 textbook questions

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