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

Although family history is a risk factor for pancreatic adenocarcinoma, much of the genetic etiology of this disease remains unknown. While genome-wide association studies have identified some common single nucleotide polymorphisms (SNPs) associated with pancreatic cancer risk, these SNPs do not exp...

Descripción completa

Detalles Bibliográficos
Autores principales: Willis, Jason A., Mukherjee, Semanti, Orlow, Irene, Viale, Agnes, Offit, Kenneth, Kurtz, Robert C., Olson, Sara H., Klein, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923159/
https://www.ncbi.nlm.nih.gov/pubmed/24592275
http://dx.doi.org/10.3389/fgene.2014.00029

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923159/
https://www.ncbi.nlm.nih.gov/pubmed/24592275
http://dx.doi.org/10.3389/fgene.2014.00029

Ejemplares similares