S Warter, J V Ruch, M Lehmann. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdolescentChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 4-5Cri-du-Chat Syndrome/geneticsFemaleHumansIntellectual Disability/geneticsKaryotypingMaleRecombination, Genetic
Year: 1973 PMID: 4768111 DOI: 10.1007/bf00273339
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348