A E Harding, C M Hall, M Baraitser. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultBone Diseases, Developmental/diagnostic imagingBone Diseases, Developmental/geneticsChild, PreschoolEar, External/abnormalitiesFace/abnormalitiesFemaleGenes, DominantHearing Loss/geneticsHearing Loss, Conductive/geneticsHumansPedigreeRadiographyRadius/abnormalitiesSyndrome
Year: 1982 PMID: 7077621 PMCID: PMC1048839 DOI: 10.1136/jmg.19.2.110
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318