Molecular biology of steroid hydroxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health
Reference58 articles.
1. Clinical and endocrinological aspects of 21-hydroxylase deficiency;New;Ann NY Acad Sci,1985
2. Congenital enzymatic defects of the adrenal;New,1985
3. Two steroid 21-hydroxylase genes are located in the murine S region;White;Nature,1984
4. Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes;Garlepp;Immunogenetics,1986
5. Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?;Stoner;Clin Endocrinol,1986
Cited by 4 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. Regulation of Steroid 17α-Hydroxylase in Adrenocortical Cells in Culture;Endocrine Research;1989-01
2. Heterogeneity of the Bovine Adrenal Steroid 21-Hydroxylase;Endocrine Research;1989-01
3. Steroid and xenobiotic effects on the adrenal cortex: mediation by oxidative and other mechanisms;Free Radical Biology and Medicine;1989-01
4. Literature reviews;Adolescent and Pediatric Gynecology;1989
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