E Sweeney, I Peart, M Tofeig, B Kerr. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome DeletionChromosomes, Human, Pair 17/geneticsDevelopmental Disabilities/geneticsFemaleHumansInfantMaleSyndromeTetralogy of Fallot/genetics
Year: 1999 PMID: 10874646 PMCID: PMC1734392
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318