Cite
HARVARD Citation
Bolli, N. et al. (2017). Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles. Cancer. 123 (19), pp. 3701-3708. [Online].
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Bolli, N. et al. (2017). Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles. Cancer. 123 (19), pp. 3701-3708. [Online].