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Gonadal Dysgenesis Without Adrenal Insufficiency in a 46, XY Patient Heterozygous for the Nonsense C16X Mutation: A Case of SF1 Haploinsufficiency
Mallet, Delphine, Bretones, Patricia, Michel-Calemard, Laurence, Dijoud, Frederique, David, Michel, Morel, YvesVolume:
89
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jc.2004-0670
Date:
October, 2004
File:
PDF, 1.42 MB
english, 2004