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Symptomatic Heterozygotes and Prenatal Diagnoses in a Nonconsanguineous Family with Syndromic Combined Pituitary Hormone Deficiency Resulting from Two Novel LHX3 Mutations
Sobrier, Marie-Laure, Brachet, Cécile, Vié-Luton, Marie-Pierre, Perez, Christelle, Copin, Bruno, Legendre, Marie, Heinrichs, Claudine, Amselem, SergeVolume:
97
Language:
english
Journal:
The Journal of Clinical Endocrinology & Metabolism
DOI:
10.1210/jc.2011-2095
Date:
March, 2012
File:
PDF, 691 KB
english, 2012