Predominant Sertoli cell deficiency in a 46,XY disorders of sex development patient with a new NR5A1/SF-1 mutation transmitted by his unaffected father

✍ Scribed by Pascal Philibert; Michel Polak; Ana Colmenares; Stephen Lortat-Jacob; Françoise Audran; Francis Poulat; Charles Sultan

• Book ID: 116478273
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 492 KB
• Volume: 95
• Category: Article
• ISSN: 1556-5653
• DOI: 10.1016/j.fertnstert.2010.11.035