The Diagnosis of Congenital Adrenal Hyperplasia in the Newborn by Gas Chromatography/Mass Spectrometry Analysis of Random Urine Specimens-Reference-Cited by-同舟云学术

The Diagnosis of Congenital Adrenal Hyperplasia in the Newborn by Gas Chromatography/Mass Spectrometry Analysis of Random Urine Specimens

Published:2002-08-01 Issue:8 Volume:87 Page:3682-3690
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Caulfield Michael P.¹,Lynn Thomas¹,Gottschalk Michael E.²,Jones Kenneth L.²,Taylor Norman F.³,Malunowicz Ewa M.⁴,Shackleton Cedric H. L.⁵,Reitz Richard E.¹,Fisher Delbert A.¹

Affiliation:

1. Quest Diagnostics’ Nichols Institute (M.P.C., T.L., R.E.R., D.A.F.), San Juan Capistrano, California 92690;

2. Department of Pediatrics, University of California, San Diego (M.E.G., K.L.J.), La Jolla, California 92123;

3. Department of Clinical Biochemistry, King’s College and School of Medicine (N.F.T.), London SE5 8RX, United Kingdom;

4. Department of Laboratory Diagnostics, Children’s Memorial Health Institute (E.M.M.), Warsaw, Poland;

5. Children’s Hospital Oakland Research Institute (C.H.L.S.), Oakland, California 94609

Publisher

The Endocrine Society

Subject

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

Link

http://academic.oup.com/jcem/article-pdf/87/8/3682/9156330/jcem3682.pdf

Reference33 articles.

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3. Disorders of steroid 11β-hydroxylase isoenzymes.;White;Endocr Rev,1994

4. The molecular and clinical spectrum of 3β-hydroxysteroid dehydrogenase deficiency disorder.;Pang;Trends Endocrinol Metab,1998

5. 17α-hydroxylase/17, 20 lyase deficiency: from clinical investigation to molecular definition.;Yanase;Endocr Rev,1991

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