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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Bibliographic Details
Published in:J Invest Dermatol
Main Authors: 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
Language:Inglês
Published: 2016
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Article
Online Access: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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