A family has an X-linked dominant form of congenital generalized hypertrichosis (excessive hairiness). Although the allele is

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A family has an X-linked dominant form of congenital generalized hypertrichosis (excessive hairiness). Although the allele is dominant, males are more severely affected than females. Moreover, the women in the family often have asymmetrical, hairy patches on their bodies. How does X chromosome inactivation explain this observation?

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