A G Hunter, J MacDonald, J A Evans. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » ChildChromosomes, Human/ultrastructureDiagnosis, DifferentialFragile X Syndrome/diagnosisHumansIntellectual Disability/diagnosisIntellectual Disability/geneticsKaryotypingMaleSex Chromosome Aberrations/diagnosis
Year: 1983 PMID: 6620334 PMCID: PMC1049131 DOI: 10.1136/jmg.20.4.314-a
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318