Human Genome Epidemiology Literature Finder
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Records 1 - 2 (of 2 Records) |
| Query Trace: 46, XY Disorders of Sex Development and SF1[original query] |
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| Novel Heterozygous Mutations of NR5A1 and Their Functional Characteristics in Patients with 46,XY Disorders of Sex Development without Adrenal Insufficiency. Hormone research in pædiatrics 2015 84 (2): 116-23. Woo Kyu Ha, Cheon Buwon, Kim Ja Hye, Cho Jahyang, Kim Gu-Hwan, Yoo Han-Wook, Choi Jin- |
| [Clinical and molecular characteristics of patients with 46,XY DSD due to NR5A1 gene mutations]. Problemy endokrinologii 2020 12 66 (3): 62-69. Kalinchenko Natalia Yu, Kolodkina Anna A, Raygorodskaya Nadezda Y, Tiulpakov Anatoly |
- Page last reviewed:Feb 1, 2024
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