B A Walker, L J Martyn, T Coffman. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultAlbinism/complicationsAlbinism/geneticsEye Diseases/geneticsFemaleFundus OculiHeterozygoteHumansMaleNystagmus, Pathologic/geneticsPedigreeSex ChromosomesVision Disorders/genetics
Year: 1971 PMID: 5173146
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844