A Schinzel, W Schmid. Show Affiliations »
Abstract
Mesh: See more » ChildChromosomes, Human, 13-15Chromosomes, Human, 16-18Ear, External/abnormalitiesEyelashes/abnormalitiesFemaleGrowth Disorders/geneticsHemangioma/geneticsHumansInfantIntellectual Disability/geneticsKaryotypingMaleMicrocephaly/geneticsMosaicismStaining and LabelingSyndromeTranslocation, GeneticTrisomy
Year: 1974 PMID: 4139096 DOI: 10.1007/bf00295488
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348