Monozygotic Twins with Congenital Adrenal Hyperplasia: Long-term Endocrine Evaluation and Gene Analysis
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.2003.16.4.565/pdf
Reference18 articles.
1. Role of gonadal hormones in development of the sexual phenotypes
2. Abnormal sex differentiation
3. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
4. P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.
5. Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatment
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