H B Pryor. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsDeafness/geneticsFemaleHumansInfant, NewbornPigmentation Disorders/geneticsWaardenburg Syndrome
Year: 1971 PMID: 5564164 DOI: 10.1001/archpedi.1971.02110020111020
Source DB: PubMed Journal: Am J Dis Child ISSN: 0002-922X