Congenital Adrenal Hyperplasia

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

Research output: Contribution to journalLetter

7 Citations (Scopus)

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 languageEnglish (US)
Pages (from-to)1413-1415
Number of pages3
JournalNew England Journal of Medicine
Volume317
Issue number22
DOIs
StatePublished - Nov 26 1987

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Congenital Adrenal Hyperplasia
DNA Restriction Enzymes
Enzymes
Southern Blotting
Molecular Biology
DNA
TCGA-specific type II deoxyribonucleases
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Congenital Adrenal Hyperplasia. / Miller, Walter L.; White, Perrin C.; New, Maria; Dupont, bo.

In: New England Journal of Medicine, Vol. 317, No. 22, 26.11.1987, p. 1413-1415.

Research output: Contribution to journalLetter

Miller, Walter L. ; White, Perrin C. ; New, Maria ; Dupont, bo. / Congenital Adrenal Hyperplasia. In: New England Journal of Medicine. 1987 ; Vol. 317, No. 22. pp. 1413-1415.
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