C O Carter. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Blindness/geneticsChromosome Aberrations/epidemiologyChromosome DisordersColonic Diseases/geneticsDeafness/geneticsGenes, DominantGenes, RecessiveGenetics, PopulationHumansInfant, NewbornMutationNervous System Diseases/geneticsPhenylketonurias/epidemiologyPolyps/geneticsSex Chromosome Aberrations/epidemiologyUnited Kingdom
Year: 1973 PMID: 4698902
Source DB: PubMed Journal: J Biosoc Sci ISSN: 0021-9320