Human Genome Epidemiology Literature Finder
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Query Trace: Hypokalemia and CYP17A1[original query] |
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Clinical and Genetic Characteristics of 17 ?-Hydroxylase/17, 20-Lyase Deficiency: c.985_987delTACinsAA Mutation of CYP17A1 Prevalent in the Chinese Han Population. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 Dec . Xia Junke, Liu Furong, Wu Jing, Xia Yanjie, Zhao Zhenhua, Zhao Yongjiang, Ren Huayan, Kong Xiangdo |
Reproductive endocrine characteristics and in vitro fertilization treatment of female patients with partial 17?-hydroxylase deficiency: Two pedigree investigations and a literature review. Frontiers in endocrinology 2022 13 970190. Jiang Shutian, Xu Yue, Qiao Jie, Wang Yao, Kuang Yanpi |
- Page last reviewed:Feb 1, 2024
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