Genome-Wide Assessment of the Association of Rare and Common Copy Number Variations to Testicular Germ Cell Cancer

Testicular germ cell cancer (TGCC) is one of the most heritable forms of cancer. Previous genome-wide association studies have focused on single nucleotide polymorphisms, largely ignoring the influence of copy number variants (CNVs). Here we present a genome-wide study of CNV on a cohort of 212 case...

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Detalles Bibliográficos
Autores principales: Edsgärd, Daniel, Dalgaard, Marlene D., Weinhold, Nils, Wesolowska-Andersen, Agata, Rajpert-De Meyts, Ewa, Ottesen, Anne Marie, Juul, Anders, Skakkebæk, Niels E., Skøt Jensen, Thomas, Gupta, Ramneek, Leffers, Henrik, Brunak, Søren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557397/
https://www.ncbi.nlm.nih.gov/pubmed/23372565
http://dx.doi.org/10.3389/fendo.2013.00002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3557397/
https://www.ncbi.nlm.nih.gov/pubmed/23372565
http://dx.doi.org/10.3389/fendo.2013.00002

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