Polimorfismos en genes de baja penetrancia como marcadores genéticos de riesgo de cáncer de mama familiar entre mujeres colombianas
Breast cancer is the most common female neoplasia worldwide. It´s estimated that most cases are sporadic, though between 10 to 15% of them have a positive family history of the disease. This familial predisposition has been associated with alterations i
- Autores:
-
Cifuentes Cardona, Laura Fernanda
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2023
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/50272
- Acceso en línea:
- http://www.scielo.org.co/pdf/rcien/v18n2/v18n2a04.pdf
https://hdl.handle.net/20.500.12494/50272
- Palabra clave:
-
EVALUACIÓN DEL RIESGO
CÁNCER DE MAMA FAMILIAR
POLIMORFISMO XRCC3 T241M
PRUEBAS GENÉTICAS
RAD51 G135C.
SÍNDROME DE CÁNCER DE MAMA Y OVARIO HEREDITARIO
- Rights
- openAccess
- License
- http://purl.org/coar/access_right/c_abf2
Summary: | Breast cancer is the most common female neoplasia worldwide. It´s estimated that most cases are sporadic, though between 10 to 15% of them have a positive family history of the disease. This familial predisposition has been associated with alterations i |
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