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Biology, 11.10.2020 21:01 mathibhh4

Curly hair is due to an autosomal dominant inheritance and the condition hypophosphatemia is due to an X-linked dominant allele. A woman who is heterozygous
for both curly hair and hypophposphatemia has a child with a male who has non-curly
hair and does not have the condition phyphosphatemia. What is the likelihood that they
will have a male child with non curly hair who does not have the condition
hypophosphatemia?

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