Human Biology: Concepts and Current Issues (8th Edition)
Human Biology: Concepts and Current Issues (8th Edition)
8th Edition
ISBN: 9780134042435
Author: Michael D. Johnson
Publisher: PEARSON
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Chapter 19, Problem 6AWK
Summary Introduction

To review:

The possibility of hemophilia to get inherited to female offspring as it is a sex-linked trait where mothers pass their affected gene to male offspring.

Introduction:

Hemophilia is a sex-linked or X-linked recessive disease, which is otherwise called as bleeder’s disease. A person with the affected recessive alleles lacks the blood clotting factor, which makes it difficult for the blood to clot during injury. The gene for the blood clotting factor is present in the X chromosome and it is inherited from parents to offspring. In general, two recessive alleles are necessary for the disease to get expressed and the dominant allele is represented as XH and recessive allele is represented as Xh.

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A form of hemophilia is caused by a sex-linked (X-linked) recessive gene. A phenotypically normal woman whose father had hemophilia marries a man who suffers with hemophilia.  What is the probability that their first daughter will have hemophilia?
Two forms of hemophilia are determined by genes on the X chromosome in humans. Assume that a phenotypically normal woman whose father had hemophilia is married to a normal man. What is their probability to have a son with hemophilia? (out of all children - not just the sons)
Hemophilia is a sex-linked recessive trait. A male hemophiliac and phenotypically normal female have a son with hemophilia.  They would like to have one more child. What is the probability of having a child without hemophilia? Explain using a Punnett square.   Is it possible for a girl to be born with hemophilia? Explain.
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY