Additional file 4: Table S5. of Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry
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Results from a genome-wide association analysis of CNVs overlapping gene loci. (XLSX 205 kb)
针对重叠于基因座（gene loci）的拷贝数变异（Copy Number Variations, CNVs）开展的全基因组关联分析（genome-wide association analysis）结果。（XLSX 205 KB）
创建时间：
2017-03-17
