Congenital Adrenal Hyperplasia
Open Access
- 26 November 1987
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 317 (22) , 1413-1415
- https://doi.org/10.1056/nejm198711263172211
Abstract
To the Editor: In Part I of their review on congenital adrenal hyperplasia (June 11 issue),1 White et al. discuss the steroidogenic enzymes and the clinical manifestations of disorders involving those enzymes; another detailed review has recently been published.2 The discussion by White et al. of the molecular genetics of 21-hydroxylase deficiency in Part II of their review (June 18 issue)3 is a bit more controversial. Their studies and those of most other groups have been similar: genomic DNA from patients with congenital adrenal hyperplasia was digested with the restriction endonuclease TaqI and analyzed by probing Southern blots with . . .Keywords
This publication has 14 references indexed in Scilit:
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- Molecular and clinical advances in congenital adrenal hyperplasiaThe Journal of Pediatrics, 1987
- Congenital Adrenal HyperplasiaNew England Journal of Medicine, 1987
- Congenital Adrenal HyperplasiaNew England Journal of Medicine, 1987
- Prevalence of polymorphic 21-hydroxylase gene (Ca21HB) mutations in salt-losing congenital adrenal hyperplasiaBiochemical and Biophysical Research Communications, 1987
- Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.Journal of Medical Genetics, 1986
- Gene Conversion in Salt-Losing Congenital Adrenal Hyperplasia with Absent Complement C4B Protein*Journal of Clinical Endocrinology & Metabolism, 1986
- C4B gene polymorphism detected in a human cosmid cloneImmunogenetics, 1986
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- Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.Proceedings of the National Academy of Sciences, 1985