| Literature DB >> 10826983 |
Abstract
Dissecting the genetics of common, complex disorders remains one of the great challenges in human genetics. The acceleration of human genome sequence determination, improvements in informatics, large-scale identification of single nucleotide polymorphisms and improvements in scoring technologies have now increased the feasibility of identifying polymorphisms that predispose to common disease.Entities:
Mesh:
Year: 2000 PMID: 10826983 DOI: 10.1016/s0959-437x(00)00075-7
Source DB: PubMed Journal: Curr Opin Genet Dev ISSN: 0959-437X Impact factor: 5.578