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Oxford University Press (OUP), Human Molecular Genetics, 5(27), p. 853-859

DOI: 10.1093/hmg/ddy005

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

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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