1. CD44-SLC1A2 Fusion Transcripts in Primary Colorectal Cancer
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  3. Genomic alterations in Turcot syndrome: Insights from whole exome sequencing
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  5. A Genetic Perspective on Colorectal Cancer Progression
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  7. Rare compound heterozygous mutations in gene MSH6 cause constitutive mismatch repair deficiency syndrome
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  8. Worldwide variation in lynch syndrome screening: case for universal screening in low colorectal cancer prevalence areas
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  11. Heterogenous loss of mismatch repair (MMR) protein expression: a challenge for immunohistochemical interpretation and microsatellite instability (MSI) evaluation
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  12. MSH6, Past and Present and Muir–Torre Syndrome—Connecting the Dots
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  13. Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide study
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  14. Population-based Screening for Hereditary Colorectal Cancer Variants in Japan
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  15. Lynch Syndrome Caused by a Germ Line Mutation in MSH6
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  16. High tumor mutational burden and T-cell activation are associated with long-term response to anti-PD1 therapy in Lynch syndrome recurrent glioblastoma patient
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  18. Protein profiles reveal MSH6/MSH2 as a potential biomarker for hepatocellular carcinoma with microvascular invasion
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