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Tumor sequencing is useful to refine the analysis of germli..:
Van Marcke, Cédric
;
Helaers, Raphaël
;
De Leener, Anne
...
Breast Cancer Research. 22 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/s13058-020-01273-y
RT Journal T1
Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13058-020-01273-y&Exemplar=1&LAN=DE A1 Van Marcke, Cédric A1 Helaers, Raphaël A1 De Leener, Anne A1 Merhi, Ahmad A1 Schoonjans, Céline A. A1 Ambroise, Jérôme A1 Galant, Christine A1 Delrée, Paul A1 Rothé, Françoise A1 Bar, Isabelle A1 Khoury, Elsa A1 Brouillard, Pascal A1 Canon, Jean-Luc A1 Vuylsteke, Peter A1 Machiels, Jean-Pascal A1 Berlière, Martine A1 Limaye, Nisha A1 Vikkula, Miikka A1 Duhoux, François P. PB Springer Science and Business Media LLC YR 2020 SN 1465-542X JF Breast Cancer Research VO 22 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13058-020-01273-y DO https://doi.org/10.1186/s13058-020-01273-y SF ELIB - SuUB Bremen
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