Profiling of the genetic features of patients with breast, ovarian, colorectal and extracolonic cancers: Association to CHEK2 and PALB2 germline mutations.

Infante, Mar; Arranz-Ledo, Mónica; Lastra, Enrique; Olaverri, Amaya; Ferreira, Raquel; Orozco, Marta; Hernández, Lara; Martínez, Noemí; Durán, Mercedes

Infante, Mar; Arranz-Ledo, Mónica; Lastra, Enrique; Olaverri, Amaya; Ferreira, Raquel; Orozco, Marta; Hernández, Lara; Martínez, Noemí; Durán, Mercedes.

Afiliación

Infante M; Cancer Genetics Group, Unit of Excellence Institute of Biomedicine and Molecular Genetics , University of Valladolid-Spanish National Research Council (IBGM, UVa-CSIC), C/ Sanz y Forés 3, 47003 Valladolid, Spain. Electronic address: mariamar.infante@uva.es.
Arranz-Ledo M; Cancer Genetics Group, Unit of Excellence Institute of Biomedicine and Molecular Genetics , University of Valladolid-Spanish National Research Council (IBGM, UVa-CSIC), C/ Sanz y Forés 3, 47003 Valladolid, Spain.
Lastra E; Unit of Genetic Counseling in Cancer, Burgos University Hospital, Burgos, Spain.
Olaverri A; Unit of Genetic Counseling in Cancer, Rio Hortega University Hospital, Valladolid, Spain.
Ferreira R; Unit of Genetic Counseling in Cancer, Rio Hortega University Hospital, Valladolid, Spain.
Orozco M; Unit of Genetic Counseling in Cancer, Rio Hortega University Hospital, Valladolid, Spain.
Hernández L; Cancer Genetics Group, Unit of Excellence Institute of Biomedicine and Molecular Genetics , University of Valladolid-Spanish National Research Council (IBGM, UVa-CSIC), C/ Sanz y Forés 3, 47003 Valladolid, Spain.
Martínez N; Cancer Genetics Group, Unit of Excellence Institute of Biomedicine and Molecular Genetics , University of Valladolid-Spanish National Research Council (IBGM, UVa-CSIC), C/ Sanz y Forés 3, 47003 Valladolid, Spain.
Durán M; Cancer Genetics Group, Unit of Excellence Institute of Biomedicine and Molecular Genetics , University of Valladolid-Spanish National Research Council (IBGM, UVa-CSIC), C/ Sanz y Forés 3, 47003 Valladolid, Spain.

Clin Chim Acta ; 552: 117695, 2024 Jan 01.

Article en En | MEDLINE | ID: mdl-38061684

Asunto(s)

Neoplasias de la Mama; Neoplasias Colorrectales; Neoplasias Ováricas; Femenino; Humanos; Mutación de Línea Germinal/genética; Predisposición Genética a la Enfermedad; Neoplasias Ováricas/genética; Neoplasias Colorrectales/diagnóstico; Neoplasias Colorrectales/genética; Neoplasias de la Mama/genética; Pruebas Genéticas/métodos; Quinasa de Punto de Control 2/genética; Proteína del Grupo de Complementación N de la Anemia de Fanconi/genética

Palabras clave

CHEK2 mutations; Endometrial cancer; Gastric cancer; Hereditary Breast and Ovarian Cancer (HBOC); Lynch Syndrome (LS); Multigene panel testing; PALB2 mutations

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Neoplasias de la Mama / Neoplasias Colorrectales Límite: Female / Humans Idioma: En Revista: Clin Chim Acta Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos

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