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Common variations in BARD1 influence susceptibility to high-risk neuroblastoma
We conducted a SNP-based genome-wide association study (GWAS) focused on the high-risk subset of neuroblastoma1. As our previous unbiased GWAS showed strong association of common 6p22 SNP alleles with aggressive neuroblastoma2, we now restricted our analysis to 397 high-risk cases compared to 2,043...
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| Autors principals: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2009
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2753610/ https://ncbi.nlm.nih.gov/pubmed/19412175 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.374 |
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