M Higurashi, P E Conen. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » AdolescentAdultCells, CulturedChildChild, PreschoolChromatidsChromosome AberrationsChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 21-22 and YChromosomes, Human, 6-12 and XCri-du-Chat Syndrome/geneticsCytogeneticsFemaleFibroblasts/cytologyHumansInfantInfant, NewbornKlinefelter Syndrome/geneticsLymphocytes/cytologyMaleMitosisPolyploidySex Chromosome AberrationsTrisomyTurner Syndrome/genetics
Year: 1971 PMID: 5127016 DOI: 10.1159/000130147
Source DB: PubMed Journal: Cytogenetics ISSN: 0011-4537