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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Main Authors: 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
格式: Artigo
語言:Inglês
出版: Frontiers Media S.A. 2013
主題:
Endocrinology
在線閱讀: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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