J P Fryns, E Eggermont, H Verresen, H Van den Berghe. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsChromosome Aberrations/diagnosisChromosome DisordersChromosomes, Human, 4-5DermatoglyphicsHumansInfantInfant, NewbornIntellectual Disability/geneticsKaryotypingMaleMicrocephaly/geneticsSyndrome
Year: 1973 PMID: 4725911 DOI: 10.1007/BF00295238
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348