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421 related items for PubMed ID: 10422993
1. Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing. Syngal S, Fox EA, Li C, Dovidio M, Eng C, Kolodner RD, Garber JE. JAMA; 1999 Jul 21; 282(3):247-53. PubMed ID: 10422993 [Abstract] [Full Text] [Related]
2. [Mutation analysis of hMSH2 and hMLH1 genes in Chinese hereditary nonpolyposis colorectal cancer families]. Cai Q, Sun MH, Fu G, Ding CW, Mo SJ, Cai SJ, Ren SX, Min DL, Xu XL, Zhu WP, Zhang TM, Shi DR. Zhonghua Bing Li Xue Za Zhi; 2003 Aug 21; 32(4):323-8. PubMed ID: 14514376 [Abstract] [Full Text] [Related]
3. Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds. Nakahara M, Yokozaki H, Yasui W, Dohi K, Tahara E. Cancer Epidemiol Biomarkers Prev; 1997 Dec 21; 6(12):1057-64. PubMed ID: 9419403 [Abstract] [Full Text] [Related]
4. Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer. Wang Q, Lasset C, Desseigne F, Saurin JC, Maugard C, Navarro C, Ruano E, Descos L, Trillet-Lenoir V, Bosset JF, Puisieux A. Hum Genet; 1999 Dec 21; 105(1-2):79-85. PubMed ID: 10480359 [Abstract] [Full Text] [Related]
5. Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma. Liu SR, Zhao B, Wang ZJ, Wan YL, Huang YT. World J Gastroenterol; 2004 Sep 15; 10(18):2647-51. PubMed ID: 15309712 [Abstract] [Full Text] [Related]
6. [Clinical features and hMSH2/hMLH1 germline mutation screening of Chinese hereditary nonpolyposis colorectal cancer patients]. Liu SR, Wang ZJ, Zhao B, Wan YL, Huang YT. Zhonghua Yi Xue Za Zhi; 2004 May 02; 84(9):714-7. PubMed ID: 15200905 [Abstract] [Full Text] [Related]
7. hMLH1 and hMSH2 gene mutation in Brazilian families with suspected hereditary nonpolyposis colorectal cancer. Rossi BM, Lopes A, Oliveira Ferreira F, Nakagawa WT, Napoli Ferreira CC, Casali Da Rocha JC, Simpson CC, Simpson AJ. Ann Surg Oncol; 2002 Jul 02; 9(6):555-61. PubMed ID: 12095971 [Abstract] [Full Text] [Related]
8. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene. Shin KH, Shin JH, Kim JH, Park JG. Cancer Res; 2002 Jan 01; 62(1):38-42. PubMed ID: 11782355 [Abstract] [Full Text] [Related]
9. Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Møller P, Fodde R. Am J Hum Genet; 1997 Aug 01; 61(2):329-35. PubMed ID: 9311737 [Abstract] [Full Text] [Related]
10. Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families. Wang Q, Desseigne F, Lasset C, Saurin JC, Navarro C, Yagci T, Keser I, Bagci H, Luleci G, Gelen T, Chayvialle JA, Puisieux A, Ozturk M. Int J Cancer; 1997 Dec 10; 73(6):831-6. PubMed ID: 9399661 [Abstract] [Full Text] [Related]
11. Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing. Cravo M, Afonso AJ, Lage P, Albuquerque C, Maia L, Lacerda C, Fidalgo P, Chaves P, Cruz C, Nobre-Leitão C. Gut; 2002 Mar 10; 50(3):405-12. PubMed ID: 11839723 [Abstract] [Full Text] [Related]
12. Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer. Curia MC, Palmirotta R, Aceto G, Messerini L, Verì MC, Crognale S, Valanzano R, Ficari F, Fracasso P, Stigliano V, Tonelli F, Casale V, Guadagni F, Battista P, Mariani-Costantini R, Cama A. Cancer Res; 1999 Aug 01; 59(15):3570-5. PubMed ID: 10446963 [Abstract] [Full Text] [Related]
13. [Mutations of hMLH1 and hMSH2 genes in suspected hereditary nonpolyposis colorectal cancer]. Yuan Y, Zheng S. Zhonghua Yi Xue Za Zhi; 1999 May 01; 79(5):346-8. PubMed ID: 11715474 [Abstract] [Full Text] [Related]
14. hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer. Kim JC, Kim HC, Roh SA, Koo KH, Lee DH, Yu CS, Lee JH, Kim TW, Lee HL, Beck NE, Bodmer WF. Cancer Detect Prev; 2001 May 01; 25(6):503-10. PubMed ID: 12132870 [Abstract] [Full Text] [Related]
15. Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer. Weber TK, Chin HM, Rodriguez-Bigas M, Keitz B, Gilligan R, O'Malley L, Urf E, Diba N, Pazik J, Petrelli NJ. JAMA; 2001 May 01; 281(24):2316-20. PubMed ID: 10386556 [Abstract] [Full Text] [Related]
16. 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 01; 6(12):987-91. PubMed ID: 9419392 [Abstract] [Full Text] [Related]
17. Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1. Syngal S, Fox EA, Eng C, Kolodner RD, Garber JE. J Med Genet; 2000 Sep 01; 37(9):641-5. PubMed ID: 10978352 [Abstract] [Full Text] [Related]
18. Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. Yuan Y, Han HJ, Zheng S, Park JG. Dis Colon Rectum; 1998 Apr 01; 41(4):434-40. PubMed ID: 9559627 [Abstract] [Full Text] [Related]
19. Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients. Katballe N, Christensen M, Wikman FP, Ørntoft TF, Laurberg S. Gut; 2002 Jan 01; 50(1):43-51. PubMed ID: 11772966 [Abstract] [Full Text] [Related]
20. Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome. Froggatt NJ, Koch J, Davies R, Evans DG, Clamp A, Quarrell OW, Weissenbach J, Hodgson SV, Ponder BA, Barton DE. J Med Genet; 1995 May 01; 32(5):352-7. PubMed ID: 7616541 [Abstract] [Full Text] [Related] Page: [Next] [New Search]