P Petit, J P Fryns, H van den Berghe. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome MappingChromosomes, Human, 13-15Chromosomes, Human, 6-12 and XHumansInfant, NewbornMalePhenotypeTranslocation, GeneticTrisomy
Year: 1980 PMID: 6965845
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995