A Geneix, J Goburdhun, C Fallet, G Lacroute, D Satge. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsAdultChromosomes, Human, Pair 18Chromosomes, Human, Pair 22FemaleFetus/abnormalitiesHumansKaryotypingPregnancySyndromeTranslocation, Genetic
Year: 2001 PMID: 11491314
Source DB: PubMed Journal: Genet Couns ISSN: 1015-8146