Titre:
  • Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families
Auteur:Van Marcke, Cédric; Helaers, Raphaël; De Leener, Anne; Merhi, Ahmad; Schoonjans, Céline C.A.; Ambroise, Jerome; Galant, Christine; Delreé, Paul; Rothé, Françoise; Bar, Isabelle; Khoury, Elsa; Brouillard, Pascal; Canon, Jean-Luc; Vuylsteke, Peter; Machiels, Jean Pascal; Berlière, Martine; Limaye, Nisha; Vikkula, Mikka; Duhoux, Francois F.P.
Informations sur la publication:Breast cancer research, 22, 1, 36
Statut de publication:Publié, 2020-04
Sujet CREF:Cancérologie
Mots-clés:Breast cancer
Germline
Mutational signatures
Predisposition
Second hit
Variant of unknown significance
Note générale:SCOPUS: ar.j
Langue:Anglais
Identificateurs:urn:issn:1465-5411
info:doi/10.1186/s13058-020-01273-y
info:scp/85083479368
info:pmid/32295625