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O-118 New insight into the genetic contribution of common variants to the development of extreme phenotypes of unexplained male infertility: a multicenter genome-wide association study
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Published in: | Human reproduction (Oxford) 2021-08, Vol.36 (Supplement_1) |
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Main Authors: | , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | |
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ISSN: | 0268-1161 1460-2350 |
DOI: | 10.1093/humrep/deab126.027 |