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1. Full Text Oral mucosal stigmata in hereditary-cancer syndromes: From germline mutations to distinctive clinical phenotypes and tailored therapies
by Ponti, Giovanni and Tomasi, Aldo and Manfredini, Marco and Pellacani, Giovanni
Gene, ISSN 0378-1119, 05/2016, Volume 582, Issue 1, pp. 23 - 32
Cowden syndrome | Odontogenic keratocystic tumors | Gardner syndrome | Peutz–Jeghers syndrome | Gorlin syndrome | Multiple endocrine neoplasia | Lynch/Muir–Torre syndrome | Ameloblastoma | Familial Adenomatous Polyposis (FAP) | Fordyce granules | Lynch/Muir-Torre syndrome | Peutz-Jeghers syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Peutz-Jeghers Syndrome - pathology | Humans | Peutz-Jeghers Syndrome - therapy | Muir-Torre Syndrome - therapy | Muir-Torre Syndrome - pathology | Multiple Endocrine Neoplasia - genetics | Germ-Line Mutation - genetics | Molecular Targeted Therapy | Adenomatous Polyposis Coli - pathology | Adenomatous Polyposis Coli - complications | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Mouth Mucosa - pathology | Gardner Syndrome - pathology | Genes, Tumor Suppressor | Gardner Syndrome - therapy | Gardner Syndrome - complications | Peutz-Jeghers Syndrome - complications | Peutz-Jeghers Syndrome - genetics | Multiple Endocrine Neoplasia - complications | Mouth Mucosa - metabolism | Muir-Torre Syndrome - genetics | Phenotype | Muir-Torre Syndrome - complications | Gardner Syndrome - genetics | Multiple Endocrine Neoplasia - therapy | Heterozygote | Multiple Endocrine Neoplasia - pathology | Genetic aspects | Gene mutations | Cancer | Index Medicus
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2. Full Text The Histomorphology of Lynch Syndrome–associated Ovarian Carcinomas: Toward a Subtype-specific Screening Strategy
by Chui, Michael Herman and Ryan, Paul and Radigan, Jordan and Ferguson, Sarah E and Pollett, Aaron and Aronson, Melyssa and Semotiuk, Kara and Holter, Spring and Sy, Keiyan and Kwon, Janice S and Soma, Anita and Singh, Naveena and Gallinger, Steven and Shaw, Patricia and Arseneau, Jocelyne and Foulkes, William D and Gilks, C Blake and Clarke, Blaise A
The American journal of surgical pathology, ISSN 0147-5185, 09/2014, Volume 38, Issue 9, pp. 1173 - 1181
ovarian cancer | mismatch repair | Lynch syndrome | Pathology | Life Sciences & Biomedicine | Surgery | Science & Technology | Colorectal Neoplasms, Hereditary Nonpolyposis - classification | Immunohistochemistry | Predictive Value of Tests | Microsatellite Instability | Carcinoma, Endometrioid - classification | Genetic Testing | Early Detection of Cancer - methods | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | Ovarian Neoplasms - pathology | Ovarian Neoplasms - genetics | Ovarian Neoplasms - classification | Carcinoma, Endometrioid - chemistry | Neoplasm Grading | DNA Mutational Analysis | DNA Mismatch Repair | Germ-Line Mutation | Adult | Female | Registries | Carcinoma, Endometrioid - genetics | Genetic Predisposition to Disease | Ovarian Neoplasms - chemistry | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Heredity | BRCA1 Protein - genetics | Canada | Phenotype | Lymphocytes, Tumor-Infiltrating - pathology | Biopsy | Pedigree | Aged | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry | BRCA2 Protein - genetics | Carcinoma, Endometrioid - pathology | Index Medicus
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3. Full Text Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer
by John M Carethers Elena M Stoffel
World journal of gastroenterology : WJG, ISSN 1007-9327, 2015, Volume 21, Issue 31, pp. 9253 - 9261
cancer;Lynch | Hereditary | non-polyposis | colorectal | Hereditary non-polyposis colorectal cancer | Familial colorectal cancer | Lynch-like syndrome | Constitutional mismatch repair deficiency syndrome | Hereditary colorectal cancer | Microsatellite instability | DNA mismatch repair | Familial colorectal cancer type X | Lynch syndrome | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Predictive Value of Tests | Diagnosis, Differential | Genetic Predisposition to Disease | Microsatellite Instability | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Brain Neoplasms - genetics | Heredity | Phenotype | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | DNA Mutational Analysis | Pedigree | DNA Mismatch Repair | Biomarkers, Tumor - genetics | Neoplastic Syndromes, Hereditary - genetics | Mutation | Index Medicus | Topic Highlight
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4. Full Text Current and future role of genetic screening in gynecologic malignancies
by Ring, Kari L., MD and Garcia, Christine, MD and Thomas, Martha H., MS and Modesitt, Susan C., MD
American journal of obstetrics and gynecology, ISSN 0002-9378, 2017, Volume 217, Issue 5, pp. 512 - 521
Obstetrics and Gynecology | BRCA | risk reduction | screening | ovarian cancer | high risk | endometrial cancer | hereditary cancer | cervical cancer | Lynch syndrome | Life Sciences & Biomedicine | Obstetrics & Gynecology | Science & Technology | Genetic Testing | DNA Polymerase III - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Li-Fraumeni Syndrome - diagnosis | DNA Mismatch Repair - genetics | Tumor Suppressor Protein p53 - genetics | Genital Neoplasms, Female - diagnosis | Li-Fraumeni Syndrome - genetics | Epithelial Cell Adhesion Molecule - genetics | Genes, BRCA2 | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Genital Neoplasms, Female - genetics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | MutL Protein Homolog 1 - genetics | Peutz-Jeghers Syndrome - diagnosis | Lynch Syndrome II - diagnosis | Mismatch Repair Endonuclease PMS2 - genetics | Gene mutations | Endometrial cancer | Diagnosis | Cervical cancer | Genetic screening | Cancer | Ovarian cancer | Index Medicus | Abridged Index Medicus
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5. Full Text Molecular pathology of Lynch syndrome
by Cerretelli, Guia and Ager, Ann and Arends, Mark J and Frayling, Ian M
The Journal of pathology, ISSN 0022-3417, 04/2020, Volume 250, Issue 5, pp. 518 - 531
colorectal cancer | gene database | immunotherapy | endometrial cancer | apoptosis | DNA mismatch repair | Lynch syndrome | gene variant interpretation | immunoediting | Pathology | Oncology | Life Sciences & Biomedicine | Science & Technology | Colon cancer | Endometrial cancer | Oncology, Experimental | Immunotherapy | Development and progression | Research | Cancer | MLH1 protein | Prophylaxis | MSH2 protein | DNA repair | MSH6 protein | Databases | Immune checkpoint | Mismatch repair | Endometrium | Apoptosis | Tumors | Immune system | Index Medicus
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6. Full Text Update on Lynch syndrome genomics
by Peltomäki, Päivi
Familial cancer, ISSN 1389-9600, 7/2016, Volume 15, Issue 3, pp. 385 - 393
Human Genetics | Biomedicine | Epimutation | Cancer Research | Tumor spectrum | Mutation | Epidemiology | Biomedicine general | DNA mismatch repair | Lynch syndrome | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Microsatellite Instability | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Genomics | Humans | DNA Repair Enzymes - genetics | MutS Homolog 2 Protein - genetics | DNA Mismatch Repair - genetics | DNA-Binding Proteins - genetics | DNA Methylation | Phenotype | MutL Protein Homolog 1 - genetics | Germ-Line Mutation | Mismatch Repair Endonuclease PMS2 - genetics | Proteins | Gene mutations | Colorectal cancer | Index Medicus | Original
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7. Full Text Cancer risk in Lynch Syndrome
by Barrow, Emma and Hill, James and Evans, D Gareth
Familial cancer, ISSN 1389-9600, 6/2013, Volume 12, Issue 2, pp. 229 - 240
Human Genetics | Statistical bias | Biomedicine | Lynch Syndrome | Hereditary nonpolyposis colorectal cancer (HNPCC) | Familial relative risk | Risk reduction | Cancer Research | Epidemiology | Biomedicine general | <