A Preto, E Lenzini, P Drigo, G Fasoli, A De Pascale. Show Affiliations »
Abstract
Mesh： See more » Abnormalities, Multiple/geneticsChromosomes, Human, 16-18Chromosomes, Human, 6-12 and XDermatoglyphicsHumansInfantTranslocation, GeneticTrisomy
Year: 1977 PMID： 613694 DOI： 10.1017/s0001566000009776
Source DB: PubMed Journal: Acta Genet Med Gemellol (Roma) ISSN： 0001-5660