A Case of Male Pseudohermaphroditism due to 17α-Hydroxylase Deficiency and Hormonal Profiles in the Nuclear Family*-Reference-Cited by-同舟云学术

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A Case of Male Pseudohermaphroditism due to 17α-Hydroxylase Deficiency and Hormonal Profiles in the Nuclear Family*

Published:1990-08 Issue:2 Volume:71 Page:523-529
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

ROHMER VINCENT,BARBOT NELLY,BERTRAND PIERRE,NAHOUL KHALIL,BIGORGNE JEAN-CLAUDE,FOREST MAGUELONE G.

Publisher

The Endocrine Society

Subject

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

Link

http://academic.oup.com/jcem/article-pdf/71/2/523/10509409/jcem0523.pdf

Cited by 8 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. Diagnosis and Treatment of Disorders of Sexual Development;Endocrinology;2010

2. DISORDERS OF SEX DEVELOPMENT;Pediatric Urology;2010

3. Anomalies du développement sexuel 46,XY (anciennement pseudohermaphrodismes masculins);EMC - Endocrinologie - Nutrition;2009-01

4. Premature adrenal cortical dysfunction in mandibuloacral dysplasia: A progeroid-like syndrome;American Journal of Medical Genetics;2000

5. Disorders of Steroid 17α-Hydroxylase Deficiency;Endocrinology and Metabolism Clinics of North America;1994-06

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