R M Liberfarb, T Hirose. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAgedChildChild, PreschoolCleft Palate/geneticsFemaleGenes, DominantHearing Loss, Sensorineural/geneticsHumansInfantJaw Abnormalities/geneticsJoint Diseases/geneticsMaleMaxilla/abnormalitiesMiddle AgedPhenotypeRetinal Degeneration/geneticsRetinal Detachment/geneticsSyndrome
Year: 1982 PMID: 7171772
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844