Cargando…
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort
The underlying genetic cause of colorectal cancer (CRC) can be identified for 5-10% of all cases, while at least 20% of CRC cases are thought to be due to inherited genetic factors. Screening for highly penetrant mutations in genes associated with Mendelian cancer syndromes using next-generation seq...
Autores principales: | Raskin, Leon, Guo, Yan, Du, Liping, Clendenning, Mark, Rosty, Christophe, Lindor, Noralane M., Gruber, Stephen B., Buchanan, Daniel D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706810/ https://www.ncbi.nlm.nih.gov/pubmed/29212164 http://dx.doi.org/10.18632/oncotarget.18596 |
Ejemplares similares
-
Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry
por: Ward, Robyn L., et al.
Publicado: (2013) -
Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort
por: Rosty, Christophe, et al.
Publicado: (2016) -
Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome)
por: Buchanan, Daniel D, et al.
Publicado: (2014) -
Disclosing genetic research results: experiences of the Colon Cancer Family Registry
por: Keogh, Louise, et al.
Publicado: (2011) -
Genetic Variations in SMAD7 Are Associated with Colorectal Cancer Risk in the Colon Cancer Family Registry
por: Jiang, Xuejuan, et al.
Publicado: (2013)