P S Harper, E M Williams. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Ethnic GroupsGenetic Diseases, Inborn/epidemiologyGenetics, PopulationHumansLeukodystrophy, Metachromatic/geneticsNystagmus, Pathologic/congenitalPhenylketonurias/geneticsWales
Year: 1975 PMID: 48718 DOI: 10.1016/s0140-6736(75)91995-9
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321