B A Miller, M S Jaafar, H Capo. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Abnormalities, MultipleCataract/complicationsCataract/geneticsChromosome DeletionChromosomes, Human, Pair 14FemaleHumansInfant, Newborn
Year: 1992 PMID: 1497515 DOI: 10.1001/archopht.1992.01080200033015
Source DB: PubMed Journal: Arch Ophthalmol ISSN: 0003-9950