R M Liberfarb, T Hirose, L B Holmes. Show Affiliations »
Abstract
Mesh: See more » AdolescentAdultAgedChildChild, PreschoolFace/abnormalitiesFemaleGenes, DominantHumansInfantMaleMiddle AgedMyopia/geneticsPhenotypeRetinal Degeneration/geneticsRetinal Detachment/etiologySyndrome
Year: 1979 PMID: 526576
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844