Related content

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

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite

Genotyping of a Chinese family with 46,XX and 46,XY 17-hydroxylase deficiency

By Tian Qinjie   Yao Fengxia   Sha Guihua   Huang Shangzhi   Tseng Hung   Schindler Adolf  

Gynecological Endocrinology, Vol. 25, Iss. 8, 2009-08 ,pp. : 485-490

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite

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

Informa Healthcare

Access to resources Recommend Favorite