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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Counseling and CYP17A1[original query]
Giant bilateral adrenal myelolipomas in two Chinese families with congenital adrenal hyperplasia.
Endocrine connections 2018 10 7 (11): 1136-41.
Liu Qiuli, Wang Lin-Ang, Su Jian, Tong Dali, Lan Weihua, Wang Luofu, Liu Gaolei, Zhang Jun, Zhang Victor Wei, Zhang Dianzheng, Chen Rongrong, Zhu Qingyi, Jiang J
[Clinical and genetic analysis of a patient with 17-hydroxylase/17,20-lyase deficiency].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 8 37 (9): 997-1000.
Zeng Yu, Mei Libin, Liang Lei, He Xuemei, Gao Haijie, Lin Shaobin, Huang Lingling, Li Pi
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
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