Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3935576 | Fertility and Sterility | 2011 | 13 Pages |
Abstract
When the 13 most common IHH/KS genes are studied, the overall prevalence of digenic gene mutations in IHH/KS was 12.5%. In addition, approximately 30% of patients without a known mutation had a mutation in a single gene. With the current state of knowledge, these findings suggest that most IHH/KS patients have a monogenic etiology.
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Authors
Samuel D. M.S., Hyung-Goo Ph.D., Elizabeth M. B.S., Tiera B.S., Lynn P. M.S., David P. M.D., Richard J. M.D., Lawrence C. M.D.,