Newborn Screening for Congenital Adrenal Hyperplasia in New Zealand, 1994–2013

Author:

Heather Natasha L.1,Seneviratne Sumudu N.2,Webster Dianne3,Derraik José G. B.2,Jefferies Craig1,Carll Joan3,Jiang Yannan4,Cutfield Wayne S.2,Hofman Paul L.2

Affiliation:

1. Starship Children's Hospital (N.L.H., C.J.), 1023 Auckland, New Zealand;

2. Liggins Institute (S.N.S., J.G.B.D., W.S.C., P.L.H.), 1142 Auckland, New Zealand;

3. New Zealand National Screening Unit (D.W., J.C.), Ministry of Health, 1051 Auckland, New Zealand

4. Department of Statistics (Y.J.), University of Auckland, 1142 Auckland, New Zealand;

Publisher

The Endocrine Society

Subject

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

Reference32 articles.

1. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Pediatrics,1988

2. Congenital adrenal hyperplasia;Merke;Lancet,2005

3. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000

4. Microfilter paper method for 17α-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia;Pang;J Clin Endocrinol Metab,1977

5. Neonatal biochemical screening for disease;Clague;Clin Chim Acta,2002

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