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

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: A Case Report

By Malan Valrie   Gesny R.   Morichon-Delvallez N.   Aubry M.C.   Benachi A.   Sanlaville D.   Turleau C.   Bonnefont J.P.   Fekete-Nihoul C.   Vekemans M.  

Human Reproduction, Vol. 22, Iss. 4, 2007-04 ,pp. : 1037-1041

Oxford University Press

Access to resources Recommend Favorite

Phenotypic variation in a Chinese family with 46,XY and 46,XX 17α-hydroxylase deficiency

By Bee Yong Mong   Manju Chandran   Papari-Zareei Mahboubeh   Auchus Richard J.  

Gynecological Endocrinology, Vol. 28, Iss. 4, 2012-04 ,pp. : 322-325

Informa Healthcare

Access to resources Recommend Favorite

XX Germ Cells: The Difference Between an Ovary and a Testis

By Whitworth D.J.  

Trends in Endocrinology and Metabolism, Vol. 9, Iss. 1, 1998-01 ,pp. : 2-6

Elsevier

Access to resources Recommend Favorite

A successful pregnancy outcome using frozen testicular sperm from a chimeric infertile male with a 46, XX/46, XY karyotype: Case report

By Sugawara Nobuo  

Human Reproduction, Vol. 20, Iss. 1, 2005-01 ,pp. : 147-148

Oxford University Press

Access to resources Recommend Favorite