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SNPs in cancer research and treatment

Genetic variation in the human genome is an emerging resource for studying cancer, a complex set of diseases characterised by both environmental and genetic contributions. The number of common germ-line variants is great, on the order of 10–15 million per person, and represents a remarkable opportun...

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Detalles Bibliográficos
Autores principales: Erichsen, H C, Chanock, S J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2410167/
https://www.ncbi.nlm.nih.gov/pubmed/14970847
http://dx.doi.org/10.1038/sj.bjc.6601574