C Vadasz. Show Affiliations »
Abstract
Mesh: See more » Genetic Diseases, Inborn/geneticsGenetic VariationHumansMutagenesisPhenotypeQuantitative Trait, Heritable
Year: 2000 PMID: 11101831 PMCID: PMC1797891 DOI: 10.1038/82506
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330