Worldwide Experience in Newborn Screening for Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency-Reference-Cited by-同舟云学术

Worldwide Experience in Newborn Screening for Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Published:1988-12 Issue:6 Volume:140 Page:1606-1606
ISSN:0022-5347
Container-title:Journal of Urology
language:en
Short-container-title:Journal of Urology

Author:

Pang S.¹²³⁴⁵,Wallace M.A.¹²³⁴⁵,Hofman L.¹²³⁴⁵,Thuline H.C.¹²³⁴⁵,Dorche C.¹²³⁴⁵,Lyon I.C.T.¹²³⁴⁵,Dobbins R.H.¹²³⁴⁵,Kling S.¹²³⁴⁵,Fujieda K.¹²³⁴⁵,Suwa S.¹²³⁴⁵

Affiliation:

1. Department of Pediatrics, University of Illinois, College of Medicine, Chicago, Illinois

2. Royal Infirmary and Stobill General Hospital, Glasgow, Scotland

3. Department of Human Services, State Laboratory of Public Health, Seattle, Washington

4. Centre de Depistage Neonatal, Hôpital Debrousse, Lyon, France

5. National Testing Center, Auckland, New Zealand

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Urology

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