F H Menko, P J Stouthart. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, Pair 1/ultrastructureChromosomes, Human, Pair 18/ultrastructureFace/abnormalitiesFemaleHumansInfant, NewbornIntellectual Disability/geneticsPhenotypeSyndromeTranslocation, Genetic
Year: 1992 PMID: 1404306 PMCID: PMC1016114 DOI: 10.1136/jmg.29.9.679-b
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318