B G Kousseff. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdolescentChild, PreschoolFemaleGenetic LinkageHumansHydrocephalus/geneticsIntellectual Disability/geneticsMaleOrofaciodigital Syndromes/geneticsX Chromosome
Year: 1982 PMID: 7081302 DOI: 10.1002/ajmg.1320110317
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299