Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families.

Authors : Van Marcke C, Helaers R, De Leener A, Merhi A, Schoonjans CA, Ambroise J, Galant C, Delrée P, Rothé F, Bar I, Khoury E, Brouillard P, Canon JL, Vuylsteke P, Machiels JP, Berlière M, Limaye N, Vikkula M, Duhoux FP
Year : 2020
Journal : Breast Cancer Res
Volume : 22
Pages : 36