M Fitchett, M Seabright. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Chromosome DeletionFemaleFragile X Syndrome/geneticsHumansSex Chromosome Aberrations/geneticsX Chromosome
Year: 1984 PMID: 6542142 PMCID: PMC1049320 DOI: 10.1136/jmg.21.5.373
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318