Tumor sequencing is useful to reclassify germline variants in unexplained high-risk breast cancer
(2019) San Antonio Breast Cancer Symposium — Location: San Antonio (10.December.2019)
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van Marcke de Lummen, C. J., Helaers, R., Schoonjans, C., Berlière, M., De Leener, A., canon, J.-L., Vuylsteke, P., Machiels, J.-P., Limaye, N., Vikkula, M., & Duhoux, F. (2019). Tumor sequencing is useful to reclassify germline variants in unexplained high-risk breast cancer. San Antonio Breast Cancer Symposium, San Antonio. https://hdl.handle.net/2078.5/169651