Your browser doesn't support javascript.
loading
In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation.
Borras, Ester; Chang, Kyle; Pande, Mala; Cuddy, Amanda; Bosch, Jennifer L; Bannon, Sarah A; Mork, Maureen E; Rodriguez-Bigas, Miguel A; Taggart, Melissa W; Lynch, Patrick M; You, Y Nancy; Vilar, Eduardo.
Afiliación
  • Borras E; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Chang K; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Pande M; Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Cuddy A; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Bosch JL; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Bannon SA; Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Mork ME; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Rodriguez-Bigas MA; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Taggart MW; Clinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Lynch PM; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • You YN; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Vilar E; Department of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Prev Res (Phila) ; 10(10): 580-587, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28765196
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Simulación por Computador / Neoplasias Colorrectales Hereditarias sin Poliposis / Proteínas de Unión al ADN / Reparación de la Incompatibilidad de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Prev Res (Phila) Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Simulación por Computador / Neoplasias Colorrectales Hereditarias sin Poliposis / Proteínas de Unión al ADN / Reparación de la Incompatibilidad de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Prev Res (Phila) Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article