C Hooft, P Haentjens, E Orye, P Kluyskens, G D'Hont. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, MultipleChildChromosome Aberrations/pathologyChromosome DisordersChromosome MappingChromosomes, Human, 16-18DermatoglyphicsDwarfism/geneticsFemaleFollow-Up StudiesHumansIntellectual Disability/geneticsKaryotyping
Year: 1968 PMID: 5747161
Source DB: PubMed Journal: Acta Paediatr Belg ISSN: 0001-6535