Related content

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

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 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

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

Molecular study of five Chinese patients with 46XX partial 17a-hydroxylase/17,20-lyase deficiency

By Tian Qinjie   Yao Fengxia   Zhang Yiwen   Tseng Hung   Lang Jinghe  

Gynecological Endocrinology, Vol. 28, Iss. 3, 2012-03 ,pp. : 234-238

Informa Healthcare

Access to resources Recommend Favorite