Rare germline copy number variations and disease susceptibility in familial melanoma

Mounting evidence suggests that copy number variations (CNVs) can contribute to cancer susceptibility. The main goal of this study was to evaluate the role of germline CNVs in melanoma predisposition in high-risk melanoma families. We used genome-wide tiling comparative genomic hybridization and SNP...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Invest Dermatol
मुख्य लेखकों: Shi, Jianxin, Zhou, Weiyin, Zhu, Bin, Hyland, Paula L, Bennett, Hunter, Xiao, Yanzi, Zhang, Xijun, Burke, Laura S, Song, Lei, Hsu, Chih Hao, Yan, Chunhua, Chen, Qingrong, Meerzaman, Daoud, Dagnall, Casey L, Burdette, Laurie, Hicks, Belynda, Freedman, Neal D, Chanock, Stephen J, Yeager, Meredith, Tucker, Margaret A, Goldstein, Alisa M, Yang, Xiaohong R
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2016
विषय:
Article
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC5123914/
https://ncbi.nlm.nih.gov/pubmed/27476724
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jid.2016.07.023
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