Congenital Adrenal Hyperplasia

Walter L. Miller; Perrin C. White; Maria New; bo Dupont

doi:10.1056/NEJM198711263172211

Congenital Adrenal Hyperplasia

Walter L. Miller, Perrin C. White, Maria New, bo Dupont

Research output: Contribution to journal › Letter › peer-review

9 Scopus citations

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…

Original language	English (US)
Pages (from-to)	1413-1415
Number of pages	3
Journal	New England Journal of Medicine
Volume	317
Issue number	22
DOIs	https://doi.org/10.1056/NEJM198711263172211
State	Published - Nov 26 1987

ASJC Scopus subject areas

General Medicine

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title = "Congenital Adrenal Hyperplasia",

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…",

author = "Miller, {Walter L.} and White, {Perrin C.} and Maria New and bo Dupont",

year = "1987",

month = nov,

day = "26",

doi = "10.1056/NEJM198711263172211",

language = "English (US)",

volume = "317",

pages = "1413--1415",

journal = "New England Journal of Medicine",

issn = "0028-4793",

publisher = "Massachussetts Medical Society",

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T1 - Congenital Adrenal Hyperplasia

AU - Miller, Walter L.

AU - White, Perrin C.

AU - New, Maria

AU - Dupont, bo

PY - 1987/11/26

Y1 - 1987/11/26

N2 - 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…

AB - 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…

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DO - 10.1056/NEJM198711263172211

M3 - Letter

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JO - New England Journal of Medicine

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ER -

Congenital Adrenal Hyperplasia

Abstract

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