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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב: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
פורמט: Artigo
שפה:Inglês
יצא לאור: 2016
נושאים:
Article
גישה מקוונת: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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