首页 | 本学科首页   官方微博 | 高级检索  
     


Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility
Authors:Giovanna Vinci M.D.   Ph.D.   Raja Brauner M.D.   Ph.D.   Attila Tar M.D.   Hassan Rouba Ph.D.   Jayesh Sheth Ph.D.   Frenny Sheth Ph.D.   Celia Ravel M.D.   Ph.D.   Ken McElreavey Ph.D.  Anu Bashamboo Ph.D.
Affiliation:a Human Developmental Genetics, Institut Pasteur, Paris, France
b Université Paris Descartes and AP-HP, Hôpital Bicêtre, Unité d'Endocrinologie pédiatrique, Le Kremlin Bicêtre, France
c Heim Pál Children's Hospital, Budapest, Hungary
d Human Genetics Unit, Institut Pasteur of Morocco, Casablanca, Morroco
e Foundation For Research in Genetics and Endocrinology, FRIGE, House, Satellite, Ahmedabad, Gujarat, India
f UPMC Univ Paris, Paris, France
g AP-HP, Hôpital Tenon, Service d'Histologie Biologie de la Reproduction, Paris, France
Abstract:
Keywords:46,XY DSD   male infertility   TSPYL1, testis
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号