A J Ebbin, M G Wilson, J W Towner, I Forsman. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, MultipleBlood Cells/cytologyBone Marrow CellsChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 1-3Chromosomes, Human, 21-22 and YDermatoglyphicsFemaleFibroblasts/cytologyHumansInfantIntellectual Disability/geneticsKaryotypingMouth Mucosa/cytologyPedigreePhenotypeSex Chromatin
Year: 1971 PMID: 5149540 PMCID: PMC1469092 DOI: 10.1136/jmg.8.4.536
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318