A gender-specific association of CNV at 6p21.3 with NPC susceptibility(†)

Copy number variations (CNVs), a major source of human genetic polymorphism, have been suggested to have an important role in genetic susceptibility to common diseases such as cancer, immune diseases and neurological disorders. Nasopharyngeal carcinoma (NPC) is a multifactorial tumor closely associa...

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Autores principales: Tse, Ka-Po, Su, Wen-Hui, Yang, Min-lee, Cheng, Hsiao-Yun, Tsang, Ngan-Ming, Chang, Kai-Ping, Hao, Sheng-Po, Yao Shugart, Yin, Chang, Yu-Sun
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2011
Materias:
Association Studies Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3146013/
https://ncbi.nlm.nih.gov/pubmed/21536588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr191
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