E Latta, J J Hoo. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsChromosomes, Human, 16-18DermatoglyphicsFemaleHumansInfant, NewbornKaryotypingSkull/abnormalitiesStaining and LabelingSyndromeTrisomy
Year: 1974 PMID: 4135958 DOI: 10.1007/bf00285107
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348