W G Pearce. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdolescentAdultCataract/geneticsChildChild, PreschoolChromosomes, Human, 6-12 and XCorneal Opacity/geneticsDwarfism/geneticsEye Diseases/geneticsFacial ExpressionFemaleHumansInfantMaleNystagmus, Pathologic/geneticsRetinitis Pigmentosa/geneticsStrabismus/geneticsTrisomy
Year: 1972 PMID: 4652816
Source DB: PubMed Journal: Can J Ophthalmol ISSN: 0008-4182 Impact factor: 1.882