Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleScreening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure.AuthorsHarrison, Steven M.; Campbell, Ian M.; Keays, Melise; Granberg, Candace F.; Villanueva, Carlos; Tannin, Grace; Zinn, Andrew R.; Castrillon, Diego H.; Shaw, Chad A.; Stankiewicz, Pawel; Baker, Linda A.PublicationAmerican Journal of Medical Genetics. Part A, 2013, Vol 161A, Issue 10, p2487ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.36084