C H Tay. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdolescentAdultAgedChild, PreschoolDeafness/geneticsFemaleHumansInfantMaleParalyses, Familial Periodic/complicationsPedigreePigmentation Disorders/geneticsWaardenburg Syndrome/complications
Year: 1971 PMID: 5580938 PMCID: PMC2466925 DOI: 10.1136/pgmj.47.548.354
Source DB: PubMed Journal: Postgrad Med J ISSN: 0032-5473 Impact factor: 2.401