S Gilgenkrantz, J Sapelier, M Thiriet, C Kahn, M Pierson. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 16-18Chromosomes, Human, 6-12 and XDermatoglyphicsFemaleHumansInfantInfant, NewbornKaryotypingTrisomy
Year: 1967 PMID: 5300124
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995