Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5689998 | Fertility and Sterility | 2017 | 9 Pages |
Abstract
Although the prevalence of WNT4, HNF1B, and LHX1 point mutations is low in people with MRKH, the prevalence of CNVs was â¼19%. Further analysis of our large familial cohort of patients will facilitate gene discovery to better understand the complex etiology of MRKH.
Keywords
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Authors
Lacey S. B.S., Durkadin Ph.D., Yiping Ph.D., Amy C. Ph.D., Lynn P. M.S., Megan E. B.S., John A. M.D., Munire M.D., Hyung-Goo Ph.D., Ozgul M. Ph.D., Lawrence C. M.D.,