A Schinzel, K Hayashi, W Schmid. Show Affiliations »
Abstract
Entities: Species
Mesh: See more » Abnormalities, Multiple/geneticsChromosome AberrationsChromosome InversionChromosomes, Human, 6-12 and X/ultrastructureCraniofacial Dysostosis/geneticsDermatoglyphicsFibroblasts/ultrastructureHeterochromatinHumansInfant, NewbornKaryotypingLymphocytes/ultrastructureMaleMosaicismPsychomotor Disorders/geneticsStaining and LabelingTrisomy
Substances: See more » Heterochromatin
Year: 1974 PMID: 4141334 DOI: 10.1007/bf00281424
Source DB: PubMed Journal: Humangenetik ISSN: 0018-7348