Genome-wide analysis of the role of copy-number variation in pancreatic cancer risk.

Willis, Jason A; Mukherjee, Semanti; Orlow, Irene; Viale, Agnes; Offit, Kenneth; Kurtz, Robert C; Olson, Sara H; Klein, Robert J

Willis, Jason A; Mukherjee, Semanti; Orlow, Irene; Viale, Agnes; Offit, Kenneth; Kurtz, Robert C; Olson, Sara H; Klein, Robert J.

Afiliación

Willis JA; Department of Medicine, Memorial Sloan-Kettering Cancer Center New York, NY, USA ; Program in Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Mukherjee S; Program in Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Orlow I; Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Viale A; Genomics Core Laboratory, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Offit K; Department of Medicine, Memorial Sloan-Kettering Cancer Center New York, NY, USA ; Program in Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Kurtz RC; Department of Medicine, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Olson SH; Department of Epidemiology and Biostatistics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.
Klein RJ; Department of Medicine, Memorial Sloan-Kettering Cancer Center New York, NY, USA ; Program in Cancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center New York, NY, USA.

Front Genet ; 5: 29, 2014.

Article en En | MEDLINE | ID: mdl-24592275

Palabras clave

CNVs; SNP microarrays; cancer risk; copy number variation; pancreatic cancer

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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Año: 2014 Tipo del documento: Article País de afiliación: Estados Unidos

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