R D Smart. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildFragile X Syndrome/epidemiologyGenetic TestingHumansSouth Africa/epidemiology
Year: 1992 PMID: 1583651 PMCID: PMC1015939 DOI: 10.1136/jmg.29.4.287-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318