H Hammami, B Daicker, E B Streiff, T Rabinowicz, M Campiche, U Wiesmann, N Herschkowitz. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, MultipleEye Diseases/geneticsGlaucoma/congenitalGrowth DisordersHumansIntellectual Disability/geneticsIntestinal AbsorptionKidney Diseases/geneticsLeukodystrophy, Metachromatic/geneticsMethodsPedigreeRenal AminoaciduriasSyndrome
Year: 1973 PMID: 4800102
Source DB: PubMed Journal: Bull Mem Soc Fr Ophtalmol ISSN: 0081-1092