N Villa, E Sala, D Colombo, M Dell'Orto, L Dalprà. Show Affiliations »
Abstract
Mesh: See more » Chromosomes, Human, Pair 1Chromosomes, Human, Pair 15Epilepsy/geneticsFemaleGrowth Disorders/geneticsHumansIntellectual Disability/geneticsKaryotypingMonosomyTranslocation, GeneticTrisomy
Year: 2000 PMID: 10991690 PMCID: PMC1734664 DOI: 10.1136/jmg.37.8.612
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318