Listar por autor "Ferreira, Raquel"

Mostrando ítems 1-3 de 3

Increased co-occurrence of pathogenic variants in hereditary breast and ovarian cancer and Lynch syndromes: A consequence of multigene panel genetic testing?

Infante Sanz, María Del Mar ; Arranz Ledo, Mónica ; Lastra, Enrique; Abella, Luis Enrique; Ferreira, Raquel; Orozco, Marta; Hernández, Lara; Martínez Martín, Noemí; Duran Dominguez, María Mercedes (2022)
Multigene germline testing usefulness instead of BRCA1/2 single screening in triple negative breast cancer cases

Arranz Ledo, Mónica ; Lastra, Enrique; Abella, Luis Enrique; Ferreira, Raquel; Orozco, Marta; Hernández, Lara; Martínez Martín, Noemí; Infante Sanz, María Del Mar ; Duran Dominguez, María Mercedes (2023)
Profiling of the genetic features of patients with breast, ovarian, colorectal and extracolonic cancers: Association to CHEK2 and PALB2 germline mutations

Infante Sanz, María Del Mar ; Arranz Ledo, Mónica ; Lastra, Enrique; Olaverri, Amaya; Ferreira, Raquel; Orozco, Marta; Hernández Sanz, Lara; Martínez Martín, Noemí; Duran Dominguez, María Mercedes (2024)