G R Sutherland. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildDiagnostic Tests, RoutineFemaleFragile X Syndrome/diagnosisHumansKaryotypingMaleSex Chromosome Aberrations/diagnosis
Year: 1984 PMID: 6694192 PMCID: PMC1049219 DOI: 10.1136/jmg.21.1.74-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318