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  1. Article

    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

    ABSTRACT: To date the molecular basis and hormonal criteria for inherited mild late-onset 3β-hydroxysteroid dehydrogenase (3β-HSD) deficiency congenital adrenal hyperplasia (CAH) have not been defined. We have...

    Ying T Chang, L I Zhang, Hala S Alkaddour, J Ian Mason, Kemming Lin… in Pediatric Research (1995)

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