I H Porter. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AllelesAnemia, Sickle Cell/bloodCystic Fibrosis/diagnosisFemaleGenes, DominantGenes, RecessiveGenetic Carrier ScreeningGenetic Diseases, Inborn/prevention & controlGenetic TestingHumansInfant, NewbornMaleMetabolism, Inborn Errors/geneticsMutationNeural Tube Defects/diagnosisPhenylketonurias/diagnosisPhenylketonurias/geneticsPregnancyPrenatal DiagnosisRiskTay-Sachs Disease/diagnosisTay-Sachs Disease/geneticsX Chromosome
Year: 1982 PMID: 6756430 DOI: 10.1146/annurev.pu.03.050182.001425
Source DB: PubMed Journal: Annu Rev Public Health ISSN: 0163-7525 Impact factor: 21.981