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HARVARD Citation
Guo, X. et al. (n.d.). Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes. Human molecular genetics. pp. 853-859. [Online].
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Guo, X. et al. (n.d.). Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes. Human molecular genetics. pp. 853-859. [Online].