L Iselius, N E Morton. Show Affiliations »
Abstract
Mesh: See more » Ataxia/geneticsChildDevelopmental Disabilities/geneticsGenetic Diseases, Inborn/geneticsHumansLaughterModels, GeneticProbabilitySeizures/geneticsSoftwareSyndrome
Year: 1991 PMID: 1714234 PMCID: PMC1683274
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025