Pages that link to "Q57316223"
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The following pages link to Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach (Q57316223):
Displaying 18 items.
- Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer (Q34633911) (← links)
- Recurrent germline mutation in MSH2 arises frequently de novo (Q35435822) (← links)
- Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing (Q35594437) (← links)
- The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumors (Q35608600) (← links)
- Assay validation for identification of hereditary nonpolyposis colon cancer-causing mutations in mismatch repair genes MLH1, MSH2, and MSH6 (Q35836701) (← links)
- Clinical characteristics and diagnosis of patients with hereditary nonpolyposis colorectal cancer (Q36178327) (← links)
- A meta-analysis of the prevalence of somatic mutations in the hMLH1 and hMSH2 genes in colorectal cancer (Q37944383) (← links)
- An MLH1 Mutation Links BACH1/FANCJ to Colon Cancer, Signaling, and Insight toward Directed Therapy (Q39639572) (← links)
- Contribution of germline MLH1 and MSH2 mutations to lobular carcinoma in situ of the breast (Q43614950) (← links)
- The phenotypic expression of three MSH2 mutations in large Newfoundland families with Lynch syndrome (Q44511151) (← links)
- Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification. (Q46602231) (← links)
- Mismatch repair gene expression defects contribute to microsatellite instability in ovarian carcinoma (Q47436506) (← links)
- The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families. (Q50894957) (← links)
- Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA. (Q52859644) (← links)
- Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients. (Q54350048) (← links)
- Low mutation rate of hMSH2 and hMLH1 in Taiwanese hereditary non-polyposis colorectal cancer. (Q54760397) (← links)
- Microsatellite Instability and Altered Expressions of MLH1 and MSH2 in Gastric Cancer (Q91897101) (← links)
- Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins (Q93083638) (← links)