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-Reference-Cited by-同舟云学术

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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

Published:1995-06 Issue:6 Volume:37 Page:820-824
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Chang Ying T,Zhang L I,Alkaddour Hala S,Mason J Ian,Lin Kemming,Yang Xiaojiang,Garibaldi Luigi R,Bourdony Carlos J,Dolan Lawrence M,Donaldson David L,Pang Songya

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Cited by 67 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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5. Adrenal Hyperandrogenism and Polycystic Ovary Syndrome;Current Pharmaceutical Design;2016-11-11

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