T A Weingeist, V Hermsen, J W Hanson, R M Bumsted, S L Weinstein, W H Olin. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAgedCataract/geneticsChildChild, PreschoolDiagnosis, DifferentialFemaleGenes, DominantHearing Loss, Sensorineural/geneticsHumansInfantInfant, NewbornJaw Abnormalities/geneticsJoint Diseases/geneticsMaleMiddle AgedMyopia/geneticsPhenotypeRetinal Degeneration/geneticsRetinal Detachment/geneticsSyndrome
Year: 1982 PMID: 7171774
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844