J Hall. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultBlindness/geneticsChild, PreschoolCleft Palate/geneticsFemaleGenes, DominantHearing Disorders/geneticsHumansMiddle AgedMucopolysaccharidosis IV/diagnostic imagingMucopolysaccharidosis IV/geneticsMyopia/geneticsPedigreePierre Robin Syndrome/geneticsRadiographyRetinal Degeneration/geneticsSyndrome
Year: 1974 PMID: 4218495
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844