C Fonatsch, S D Flatz. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsAdultAneuploidyChromosome AberrationsChromosomes, Human, 16-18Chromosomes, Human, 4-5DermatoglyphicsFemaleHumansInfantIntellectual Disability/geneticsKaryotypingMalePedigreePsychomotor Disorders/geneticsStaining and LabelingTranslocation, GeneticTrisomy
Year: 1974 PMID: 4141336 DOI: 10.1007/bf00281431
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348