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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.

Type

Journal article

Journal

Curr Opin Genet Dev

Publication Date

06/2000

Volume

10

Pages

330 - 334

Keywords

Chromosome Mapping, Genetic Diseases, Inborn, Genetics, Medical, Genome, Human, Humans, Polymorphism, Genetic