J M Opitz. Show Affiliations »
Abstract
Mesh: See more » Fragile X Syndrome/geneticsGenetic LinkageHumansIntellectual Disability/geneticsMutationSex Chromosome Aberrations/geneticsX Chromosome
Year: 1986 PMID: 3953638 DOI: 10.1002/ajmg.1320230102
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299