Papers: 10.1186/s13058-020-01273-y

https://doi.org/10.1186/s13058-020-01273-y

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

Cited by: 6
Author(s): Cédric Van Marcke, Raphaël Helaers, Anne De Leener, Mariam Ahmad, Céline A Schoonjans, Jérôme Ambroise, Christine Galant, P. Delrée, Françoise Rothé, Isabelle Bar, Elsa Khoury, Pascal Brouillard, Jean-Luc Canon, Peter Vuylsteke, Jean‐Pascal Machiels, Martine Berlière, Nisha Limaye, Miikka Vikkula, François P. Duhoux
Published: over 5 years ago

Software Mentions 2