Familial Male Pseudohermaphroditism due to 17–20- Desmolase Deficiency. I.In VivoEndocrine Studies*-Reference-Cited by-同舟云学术

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Familial Male Pseudohermaphroditism due to 17–20- Desmolase Deficiency. I.In VivoEndocrine Studies*

Published:1980-05 Issue:5 Volume:50 Page:826-833
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

FOREST MAGUELONE G.,LECORNU MARCEL,PERETTI EVELINE DE

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/50/5/826/10514081/jcem0826.pdf

Cited by 40 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

1. Genetic Disorders of the Adrenal Gland;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

2. A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2012-03-01

3. The Syndrome of 17,20 Lyase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2012-01

4. Diagnosis and Treatment of Disorders of Sexual Development;Endocrinology;2010

5. CYP17- and CYP11B-dependent steroid hydroxylases as drug development targets;Pharmacology & Therapeutics;2006-07

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