T E Kelly, J M Rary. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Bone Marrow CellsCells, CulturedCheekChild, PreschoolDiploidyFemaleFibroblasts/cytologyGrowth Disorders/geneticsHumansIntellectual Disability/geneticsKaryotypingLymphocytes/cytologyMosaicismMouth Mucosa/cytologyPolyploidySex ChromatinSyndrome
Year: 1974 PMID: 4426137 DOI: 10.1111/j.1399-0004.1974.tb00655.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438