Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family

Copy number variations (CNVs) have been shown to contribute substantially to disease susceptibility in several inherited diseases including cancer. We conducted a genome-wide search for CNVs in blood-derived DNA from 79 individuals (62 melanoma patients and 17 spouse controls) of 30 high-risk melano...

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Detalhes bibliográficos
Main Authors: Yang, Xiaohong R., Brown, Kevin, Landi, Maria T., Ghiorzo, Paola, Badenas, Celia, Xu, Mai, Hayward, Nicholas K., Calista, Donato, Landi, Giorgio, Bruno, William, Bianchi-Scarrà, Giovanna, Aguilera, Paula, Puig, Susana, Goldstein, Alisa M., Tucker, Margaret A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3288577/
https://ncbi.nlm.nih.gov/pubmed/22225770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1755-148X.2012.00969.x
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