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4. PMS2 mutations in HNPCC. Hayward BE; De Vos M; Sheridan E; Bonthron DT Clin Genet; 2004 Dec; 66(6):566-7; author reply 568. PubMed ID: 15521988 [No Abstract] [Full Text] [Related]
5. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nicolaides NC; Papadopoulos N; Liu B; Wei YF; Carter KC; Ruben SM; Rosen CA; Haseltine WA; Fleischmann RD; Fraser CM Nature; 1994 Sep; 371(6492):75-80. PubMed ID: 8072530 [TBL] [Abstract][Full Text] [Related]
6. [Combining clinical investigation with molecular genetics research: to push forward the study of hereditary colorectal carcinoma into a higher level in China]. Li S Zhonghua Yi Xue Za Zhi; 2002 Oct; 82(20):1369-70. PubMed ID: 12613476 [No Abstract] [Full Text] [Related]
7. Genetic alteration in hereditary colorectal cancer. Dionigi G; Bianchi V; Rovera F; Boni L; Annoni M; Castano P; Villa F; Dionigi R Surg Oncol; 2007 Dec; 16 Suppl 1():S11-5. PubMed ID: 18023570 [TBL] [Abstract][Full Text] [Related]
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10. Etiology, natural history, management and molecular genetics of hereditary nonpolyposis colorectal cancer (Lynch syndromes): genetic counseling implications. Lynch HT; Lemon SJ; Karr B; Franklin B; Lynch JF; Watson P; Tinley S; Lerman C; Carter C Cancer Epidemiol Biomarkers Prev; 1997 Dec; 6(12):987-91. PubMed ID: 9419392 [TBL] [Abstract][Full Text] [Related]
11. Immunohistochemistry for PMS2 and MSH6 alone can replace a four antibody panel for mismatch repair deficiency screening in colorectal adenocarcinoma. Hicks SC; Ward RL; Hawkins NJ Pathology; 2011 Jan; 43(1):84-5; author reply 85-6. PubMed ID: 21240077 [No Abstract] [Full Text] [Related]
12. Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome). Hendriks YM; Jagmohan-Changur S; van der Klift HM; Morreau H; van Puijenbroek M; Tops C; van Os T; Wagner A; Ausems MG; Gomez E; Breuning MH; Bröcker-Vriends AH; Vasen HF; Wijnen JT Gastroenterology; 2006 Feb; 130(2):312-22. PubMed ID: 16472587 [TBL] [Abstract][Full Text] [Related]
13. Clearer picture of PMS2-associated lynch syndrome is emerging. Daniels MS; Lu KH J Clin Oncol; 2015 Feb; 33(4):299-300. PubMed ID: 25534383 [No Abstract] [Full Text] [Related]
14. Molecular basis of HNPCC: mutations of MMR genes. Papadopoulos N; Lindblom A Hum Mutat; 1997; 10(2):89-99. PubMed ID: 9259192 [TBL] [Abstract][Full Text] [Related]
15. Germline PMS2 mutations: one hit or two? Gryfe R; Gallinger S Gastroenterology; 2005 May; 128(5):1506-9. PubMed ID: 15887130 [No Abstract] [Full Text] [Related]
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18. PMS2 mutations in childhood cancer. Bonthron DT; Hayward BE; De Vos M; Sheridan E Gut; 2005 Dec; 54(12):1821. PubMed ID: 16284300 [No Abstract] [Full Text] [Related]
19. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics. Lagerstedt Robinson K; Liu T; Vandrovcova J; Halvarsson B; Clendenning M; Frebourg T; Papadopoulos N; Kinzler KW; Vogelstein B; Peltomäki P; Kolodner RD; Nilbert M; Lindblom A J Natl Cancer Inst; 2007 Feb; 99(4):291-9. PubMed ID: 17312306 [TBL] [Abstract][Full Text] [Related]
20. Polymorphisms and HNPCC: PMS2-MLH1 protein interactions diminished by single nucleotide polymorphisms. Yuan ZQ; Gottlieb B; Beitel LK; Wong N; Gordon PH; Wang Q; Puisieux A; Foulkes WD; Trifiro M Hum Mutat; 2002 Feb; 19(2):108-13. PubMed ID: 11793469 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]