Genome Sequencing of Undiagnosed European Patients Suspected of Hereditary Cancer: Diagnostic Yield and Identification of Candidate Causative Variants
Nelson Martins(Universidade do Porto), Laura Valle(Institut d'Investigació Biomédica de Bellvitge), Ana Blatnik(Institut d'Investigació Biomèdica de Girona), Iris B.A.W. Te Paske(Radboud University Nijmegen), Nicoline Hoogerbrugge(Radboud University Nijmegen), Ana Berta Sousa(Administração Regional de Saúde de Lisboa e Vale do Tejo), Stefan Aretz(University of Bonn), Irene Gullo(Universidade do Porto), Richarda M. de Voer(Radboud University Nijmegen), Arvīds Irmejs(University of Parma), Pedro Amoroso Canão(Hospital de São João), Paula Rofes(Institut d'Investigació Biomédica de Bellvitge), Gabriel Capellá(Institut Català d'Oncologia), Valeria Barili(Institute of Oncology Ljubljana), José Garcia‐Pelaez(Universidade do Porto), Isabel Spier(University of Bonn), Leslie Matalonga(Centre for Genomic Regulation), Susana Fernandes(Universidade do Porto), Luzia Garrido(Hospital de São João), J Brunet(Institut d'Investigació Biomédica de Bellvitge), Carla Oliveíra(Universidade do Porto), Conxi Lázaro(Institut d'Investigació Biomédica de Bellvitge), Celina São José(Universidade do Porto), Steven Laurie(Centre for Genomic Regulation), Anna Sommer(Helmholtz Zentrum München), Sofia Maia(Instituto Português de Oncologia Francisco Gentil), Juliette Dupont(Administração Regional de Saúde de Lisboa e Vale do Tejo), Mireia Ramos-Muntada(Institut d'Investigació Biomédica de Bellvitge), R Lourenço Silva(Administração Regional de Saúde de Lisboa e Vale do Tejo), Ana Maria Pedro(Universidade do Porto), Arjen Mensenkamp(Radboud University Nijmegen), Gabriela Sousa(Riga Stradiņš University), Mariona Terradas(Universitat Autònoma de Barcelona), Janneke Schuurs-Hoeijmakers(Radboud University Nijmegen), German Demidov(Universitat Pompeu Fabra)
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