Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia*-Reference-Cited by-同舟云学术

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Pitfalls of Prenatal Diagnosis of 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia*

Published:1985-07 Issue:1 Volume:61 Page:89-97
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

PANG SONGYA,POLLACK MARILYN S.,LOO MAY,GREEN ORVILLE,NUSSBAUM ROBERT,CLAYTON GEORGE,DUPONT BO,NEW MARIA I.

Publisher

The Endocrine Society

Subject

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

Link

http://academic.oup.com/jcem/article-pdf/61/1/89/10525892/jcem0089.pdf

Cited by 63 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. Prenatal diagnosis and in utero treatment of congenital adrenal hyperplasia: An up‐to‐date comprehensive review;Prenatal Diagnosis;2024-03-06

2. Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene;Annals of Pediatric Endocrinology & Metabolism;2024-02-29

3. The history of prenatal diagnosis of congenital adrenal hyperplasia;Genetic Steroid Disorders;2023

4. Pathogenesis and Treatment of Disorders of Sexual Development;Endocrine Surgery in Children;2017-08-02

5. Prenatal Diagnosis of Congenital Adrenal Hyperplasia;Endocrinology and Metabolism Clinics of North America;2016-06

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