Hyperandrogenism in carriers of CYP21 mutations: the role of genotype
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2006.02521.x/fullpdf
Reference29 articles.
1. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
2. Congenital adrenal hyperplasias
3. Congenital Adrenal Hyperplasia
4. NEWBORN SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
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