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Article

Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease.

Disease markers - 1 Jan 2001

Chanock S

Abstract excerpt

The genomic revolution has generated an extraordinary resource, the catalog of variation within the human genome, for investigating biological, evolutionary and medical questions. Together with new, more efficient platforms for high-throughput genotyping, it is possible to begin to dissect genetic contributions to complex trait diseases, specifically examining common variants, such as the single nucleotide...

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Identifiers

PMID: 11673655
DOI: 10.1155/2001/858760
PMCID: PMC3850582

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