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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Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2013
Matèries:
Endocrinology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3557397/
https://ncbi.nlm.nih.gov/pubmed/23372565
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2013.00002
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