J Hansen. Show Affiliations »
Abstract
Entities: Chemical Disease
Mesh: See more » Blindness/complicationsChild, PreschoolChromosome AberrationsChromosomes, Human, 16-18Chromosomes, Human, 6-12 and XCytogeneticsDermatoglyphicsFemaleGenotypeHumansInfantKaryotypingMaleMental Disorders/complicationsMosaicismNystagmus, Pathologic/complicationsPhenotypeTrisomyVision Disorders/complications
Year: 1970 PMID: 5480412 DOI: 10.1007/BF01486637
Source DB: PubMed Journal: Klin Wochenschr ISSN: 0023-2173