The Molecular and Clinical Spectrum of 3β-hydroxysteroid Dehydrogenase Deficiency Disorder
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference20 articles.
1. Hypothalamic–pituitary–gonadal axis function in pubertal male and female siblings with glucocorticoid-treated non salt-wasting 3β-hydroxysteroid dehydrogenase deficiency congenital adrenal hyperplasia;Chang;J Clin Endocrinol Metab,1993
2. Absence of molecular defect in the type II 3β-hydroxysteroid dehydrogenase (3β-HSD) gene in premature pubarche children and hirsute female patients with moderately decreased adrenal 3β-HSD activity;Chang;Pediatr Res,1995
3. The role of adrenocorticotropin tests in evaluating girls with premature adrenarche and hirsutism/oligomenorrhea;Hawkins;J Clin Endocrinol Metab,1992
4. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia;Kohn;J Clin Endocrinol Metab,1982
5. Structure function and tissue-specific gene expression of 3β-hydroxysteroid dehydrogenase/Δ5-ene isomerase enzymes in classical and peripheral intracrine steroidogenic tissues;Labrie;J Steroid Biochem Mol Biol,1992
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