P H Zweifach. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » AdolescentAlopecia/etiologyChildChild, PreschoolChoroid/physiopathologyEye Diseases/congenitalFemaleHumansInfantMaleOphthalmoscopyPigmentation Disorders/congenitalRetina/physiopathologyTrisomy
Year: 1966 PMID: 5929139 DOI: 10.1016/0002-9394(66)92201-x
Source DB: PubMed Journal: Am J Ophthalmol ISSN: 0002-9394 Impact factor: 5.258