CYP17A1 mutations identified in 17 Chinese patients with 17α-hydroxylase/17,20-lyase deficiency

By Yao Fengxia   Huang Shangzhi   Kang Xiaodi   Zhang Weimin   Wang Peng   Tian Qinjie  

Gynecological Endocrinology, Vol. 29, Iss. 1, 2013-01 ,pp. : 10-15

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Homozygous CYP17A1 mutation (H373L) identified in a 46,XX female with combined 17α-hydroxylase/17,20-lyase deficiency

By Lee Mee-Hwa   Won Park Seok   Yoon Tae Ki   Shim Sung Han  

Gynecological Endocrinology, Vol. 28, Iss. 7, 2012-07 ,pp. : 573-576

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CYP17A1 gene mutations and hypertension variations found in 46, XY females with combined 17α-hydroxylase/17, 20-lyase deficiency*

By Wang Yue-Ping   Zhao Yun-Jing   Zhou Guang-Yu   He Bing  

Gynecological Endocrinology, Vol. 30, Iss. 6, 2014-06 ,pp. : 456-460

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Clinical and genetic analysis for two Chinese siblings with 17α-hydroxylase/17,20-lyase deficiency

By Zhou Qi   Wu Chaoming   Wang Liang   Zheng Jingchen   Zheng Chao   Jin Jian   Qian Yanying   Ni Li  

Gynecological Endocrinology, Vol. 28, Iss. 6, 2012-06 ,pp. : 455-459

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Partial 17α-hydroxylase/17,20-lyase deficiency-clinical report of five Chinese 46,XX cases

By Tian Qinjie   Zhang Yiwen   Lu Zhaolin  

Gynecological Endocrinology, Vol. 24, Iss. 7, 2008-01 ,pp. : 362-367

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