T Talvik, A V Mikelsaar, R Mikelsaar, M Käosaar, S Tüür. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsAutoradiographyChromosome AberrationsChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 21-22 and YChromosomes, Human, 6-12 and XDermatoglyphicsFemaleFluorescenceHumansInfantInfant, NewbornKaryotypingMalePedigreePhenotype
Year: 1973 PMID: 4763926 DOI: 10.1007/bf00278394
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348