Copy Number Variation Analysis on a Non-Hodgkin Lymphoma Case-Control Study Identifies an 11q25 Duplication Associated with Diffuse Large B-Cell Lymphoma

Recent GWAS have identified several susceptibility loci for NHL. Despite these successes, much of the heritable variation in NHL risk remains to be explained. Common copy-number variants are important genomic sources of variability, and hence a potential source to explain part of this missing herita...

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Detalles Bibliográficos
Autores principales: Conde, Lucia, Riby, Jacques, Zhang, Jianqing, Bracci, Paige M., Skibola, Christine F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4136881/
https://www.ncbi.nlm.nih.gov/pubmed/25133503
http://dx.doi.org/10.1371/journal.pone.0105382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4136881/
https://www.ncbi.nlm.nih.gov/pubmed/25133503
http://dx.doi.org/10.1371/journal.pone.0105382

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