Late-Onset 21-Hydroxylase Deficiency Is an Allelic Variant of Congenital Adrenal Hyperplasia Characterized by Attenuated Clinical Expression and Different HLA Haplotype Associations-Reference-Cited by-同舟云学术

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Late-Onset 21-Hydroxylase Deficiency Is an Allelic Variant of Congenital Adrenal Hyperplasia Characterized by Attenuated Clinical Expression and Different HLA Haplotype Associations

Published:1982 Issue:4 Volume:16 Page:193-200
ISSN:1423-0046
Container-title:Hormone Research
language:en
Short-container-title:Horm Res

Author:

Chrousos George P.,Loriaux Lynn,Mann Dean,Cutler, Jr. Gordon B.

Publisher

S. Karger AG

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

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

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3. Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency;Genetic Steroid Disorders;2014

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

5. The Adrenal Cortex;Tietz Textbook of Clinical Chemistry and Molecular Diagnostics;2012

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