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Two unrelated undervirilized 46,XY males with inherited NR5A1 variants identified by whole exome sequencing
BACKGROUND: Undervirilized 46,XY males with bifid scrotum often pose a diagnostic challenge, and the majority of cases typically do not receive a genetic diagnosis. NR5A1 mutations can be seen in 10–20% of cases and are a relatively common cause of undervirilization. METHODS: Whole-exome sequencing...
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| Yayımlandı: | Horm Res Paediatr |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5325809/ https://ncbi.nlm.nih.gov/pubmed/27553487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000448754 |
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