Pages that link to "Q51073023"
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The following pages link to Prevalence of germline MUTYH mutations among Lynch-like syndrome patients (Q51073023):
Displaying 23 items.
- The molecular basis of rectal cancer (Q35109123) (← links)
- Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome (Q35998356) (← links)
- Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients. (Q36051960) (← links)
- MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria (Q36213262) (← links)
- Screening adherence and cancer risk perceptions in colorectal cancer survivors with Lynch-like syndrome. (Q37071737) (← links)
- Evolving approach and clinical significance of detecting DNA mismatch repair deficiency in colorectal carcinoma. (Q37247809) (← links)
- Lynch syndrome: five unanswered questions (Q38367449) (← links)
- Characterization of a novel POLD1 missense founder mutation in a Spanish population (Q38743632) (← links)
- An Individual with Both MUTYH-Associated Polyposis and Lynch Syndrome Identified by Multi-Gene Hereditary Cancer Panel Testing: A Case Report (Q39020597) (← links)
- Repair of 8-oxoG:A mismatches by the MUTYH glycosylase: Mechanism, metals and medicine (Q39087831) (← links)
- Cancer screening behaviors and risk perceptions among family members of colorectal cancer patients with unexplained mismatch repair deficiency (Q39198359) (← links)
- Sebaceous Carcinoma: A Review of the Scientific Literature (Q39417272) (← links)
- Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis. (Q40174495) (← links)
- Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description (Q42081132) (← links)
- Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel (Q50588017) (← links)
- Hereditary Nonpolyposis Colorectal Cancer and Cancer Syndromes: Recent Basic and Clinical Discoveries. (Q54983718) (← links)
- DNA mismatch repair protein deficient non-neoplastic colonic crypts: a novel indicator of Lynch syndrome (Q59510505) (← links)
- Microsatellite instability in colorectal cancer (Q88619637) (← links)
- Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes (Q89393728) (← links)
- Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis (Q90331269) (← links)
- Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome (Q92403143) (← links)
- Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring (Q97550251) (← links)
- Comparison of Molecular, Clinicopathological, and Pedigree Differences Between Lynch-Like and Lynch Syndromes (Q99711644) (← links)