C Waldenmaier, W Hirsch, E König, K Shibata. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildChromosome AberrationsChromosomes, Human, 16-18Chromosomes, Human, 21-22 and YDermatoglyphicsFibroblasts/cytologyHumansIntellectual Disability/geneticsKaryotypingKlinefelter Syndrome/geneticsLymphocytes/cytologyMaleStaining and Labeling
Year: 1974 PMID: 4134628 DOI: 10.1007/bf00273370
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348