W A Manschot. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/pathologyAdolescentAdultBlindness/congenitalBlindness/pathologyChromosome Aberrations/pathologyChromosome DisordersEdema/pathologyEye AbnormalitiesEye Diseases/geneticsFemaleGenetic Diseases, Inborn/pathologyHearing DisordersHemoglobinopathies/geneticsHumansIntellectual Disability/pathologyMacula Lutea/pathologyMaleMiddle AgedMyopia/geneticsMyopia/pathologyNight Blindness/pathologyRetina/pathologyRetinal Degeneration/geneticsRetinal Degeneration/pathologyRetinal Detachment/etiologyRetinal Detachment/geneticsRetinal Detachment/pathology
Year: 1971 PMID: 4997129 DOI: 10.1159/000306280
Source DB: PubMed Journal: Ophthalmologica ISSN: 0030-3755 Impact factor: 3.250