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Abstract
Mesh: See more » Chromosome MappingGenetic Diseases, Inborn/geneticsGenetic VariationGenetics, MedicalHumansPolymorphism, Single NucleotideSocieties, Scientific
Year: 1999 PMID: 10548090 DOI: 10.1038/44432
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962