Cite
HARVARD Citation
Felicio, P. et al. (2021). Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer. Human mutation. 42 (3), pp. 290-299. [Online].
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Felicio, P. et al. (2021). Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer. Human mutation. 42 (3), pp. 290-299. [Online].