Association of a germline copy number variation at 2p24.3 and risk for aggressive prostate cancer

We searched for deletions in the germline genome among 498 aggressive prostate cancer cases and 494 controls from a population-based study in Sweden (CAPS) using Affymetrix SNP arrays. By comparing allele intensities of ∼500,000 SNP probes across the genome, a germline deletion at 2p24.3 was observe...

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Detalhes bibliográficos
Main Authors: Liu, Wennuan, Sun, Jishan, Li, Ge, Zhu, Yi, Zhang, Scott, Kim, Seong-Tae, Sun, Jielin, Wiklund, Fredrik, Wiley, Kathleen, Isaacs, Sarah D., Stattin, Pär, Xu, Jianfeng, Duggan, David, Carpten, John D., Isaacs, William B., Grönberg, Henrik, Zheng, S. Lilly, Chang, Bao-Li
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2743179/
https://ncbi.nlm.nih.gov/pubmed/19258504
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-08-3151
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