chilanka
chilanka
16.04.2020 • 
Biology

Cherubism is a rare autosomal dominant disease of the jaw. You have identified a family in which cherubism is segregating, as well as the mutation causing the disease. Through DNA testing you determine that 17 members of the family carry the mutation, but only 6 of them display cherubism. What is the penetrance of the mutation in this family?

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