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...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2013
Konular:
Endocrinology
Online Erişim: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
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!

Benzer Materyaller