C Bay, L Kerzin, B D Hall. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdultFemaleGenetic CounselingGenetic LinkageHumansHydrocephalus/epidemiologyHydrocephalus/etiologyHydrocephalus/geneticsInfant, NewbornMalePhenotypeRetrospective StudiesRiskSyndromeX Chromosome
Year: 1979 PMID: 526618
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844