M Deminatti, E Maillard, B Gosselin, J M Peltier, M F Bulteel, C Dupuis. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsBrain/pathologyChromosome Aberrations/pathologyChromosome DisordersChromosomes, Human, 21-22 and YChromosomes, Human, 6-12 and XDermatoglyphicsFemaleHumansInfantKaryotypingMyocardium/pathologyPedigreePhenotypeTrisomy
Year: 1969 PMID: 5306710
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995