A Kleczkowska1, P Decock, H van den Berghe, J P Fryns. Show Affiliations » 1. Centre for Human Genetics, University of Leuven, Belgium.
Abstract
Entities: Disease
Mesh: See more » AdolescentChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, Pair 7Facial Bones/abnormalitiesFemaleHumansIntellectual Disability/diagnosisIntellectual Disability/geneticsIntelligence/geneticsKaryotypingPhenotypePsychomotor Disorders/diagnosisPsychomotor Disorders/geneticsRepetitive Sequences, Nucleic Acid/geneticsSkull/abnormalitiesTrisomy/genetics
Year: 1994 PMID: 7888144
Source DB: PubMed Journal: Genet Couns ISSN: 1015-8146