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...

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Bibliografski detalji
Izdano u:J Invest Dermatol
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: 2016
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Article
Online pristup: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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