1. MiR-137 Targets the 3′ Untranslated Region of MSH2: Potential Implications in Lynch Syndrome-Related Colorectal Cancer
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2. Primary malignant pericardial tumour in Lynch syndrome
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3. WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
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4. Rektumkarzinom
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6. Utility of Matrix Metalloproteinases in the Diagnosis, Monitoring and Prognosis of Ovarian Cancer Patients
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7. Organization clinical decision-making programs in the local practice of the region: problematic issues that determine the choice of therapy in the progression of endometrial cancer
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8. Hereditary Cancer Syndromes and Inherited Cancer Risks
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9. Long-Term Survival of a Lynch Syndrome Patient With Eight Primary Tumors: A Case Report
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10. A clinical case of a hereditary form of colorectal cancer associated with a CHEK2 gene defect
    Ildar R. Minniakhmetov et al, 2021, Russian Journal of Oncology CrossRef
11. Neuroendocrine carcinoma of the endometrium concomitant with Lynch syndrome: A case report
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12. Hereditary Gynecologic Cancer Syndromes – A Narrative Review
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13. Molecular Pathways, Targeted Therapies, and Proteomic Investigations of Colorectal Cancer
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14. The Day-To-Day Practice of MMR and MSI Assessment in Colorectal Adenocarcinoma: What We Know and What We Still Need to Explore
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15. Inoperable de novo metastatic colorectal cancer with primary tumour in situ: Evaluating discordant responses to upfront systemic therapy of the primary tumours and metastatic sites and complications arising from primary tumours (experiences from an Irish Cancer Centre)
    Ruba Hamed et al, 2021, Molecular and Clinical Oncology CrossRef
16. Case Report: A New Subtype of Lynch Syndrome Associated With MSH2 c.1024_1026 Identified in a Chinese Family
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17. Microsatellite instability in endometrial cancer: the role of diagnostic methods and their clinical application. Expert consensus
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18. Do non-pathogenic variants of DNA mismatch repair genes modify neurofibroma load in neurofibromatosis type 1?
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