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Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes.

Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes. Hum Mol Genet. 2018 03 01; 27(5):853-859.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.