Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Molecular Biology,Biochemistry
Reference45 articles.
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2. Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society;Clayton;Horm. Res.,2002
3. Sexual function and genital sensitivity following feminizing genitoplasty for congenital adrenal hyperplasia;Crouch;J. Urol.,2008
4. Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency;David;J. Pediatr.,1984
5. Identification of non-amplifying CYP21 genes when using PCR-based diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH) affected pedigrees;Day;Hum. Mol. Genet.,1996
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