R A Pagon, J W Chandler, W R Collie, S K Clarren, J Moon, S A Minkin, J G Hall. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Cerebral Cortex/abnormalitiesEncephalocele/geneticsFemaleHumansHydrocephalus/geneticsInfantInfant, NewbornMalePedigreeRetinal Diseases/geneticsSyndrome
Year: 1978 PMID: 728564
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844