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Journal Abstract Search

396 related items for PubMed ID: 11145293

  • 1. Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome.
    Nilbert M, Fernebro J, Kristoffersson U.
    Scand J Gastroenterol; 2000 Nov; 35(11):1200-3. PubMed ID: 11145293
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  • 2. Inactivation of germline mutant APC alleles by attenuated somatic mutations: a molecular genetic mechanism for attenuated familial adenomatous polyposis.
    Su LK, Barnes CJ, Yao W, Qi Y, Lynch PM, Steinbach G.
    Am J Hum Genet; 2000 Sep; 67(3):582-90. PubMed ID: 10924409
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  • 3. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome.
    Foulkes WD.
    QJM; 1995 Dec; 88(12):853-63. PubMed ID: 8593545
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  • 4. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
    Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M.
    BMC Med Genet; 2007 Apr 05; 8():16. PubMed ID: 17411426
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  • 5. Germline hypermethylation of the APC promoter is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families.
    Romero-Giménez J, Dopeso H, Blanco I, Guerra-Moreno A, Gonzalez S, Vogt S, Aretz S, Schwartz S, Capella G, Arango D.
    Int J Cancer; 2008 Mar 15; 122(6):1422-5. PubMed ID: 18027849
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  • 6. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
    Nielsen M, Hes FJ, Nagengast FM, Weiss MM, Mathus-Vliegen EM, Morreau H, Breuning MH, Wijnen JT, Tops CM, Vasen HF.
    Clin Genet; 2007 May 15; 71(5):427-33. PubMed ID: 17489848
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  • 7. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.
    Wang D, Liang S, Zhang Z, Zhao G, Hu Y, Liang S, Zhang X, Banerjee S.
    Oncotarget; 2017 Mar 28; 8(13):21327-21335. PubMed ID: 28423518
    [Abstract] [Full Text] [Related]

  • 8. Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report.
    Khider F, Cherbal F, Boumehdi AL, Layaida K, Mahfouf H, Zebboudj F, Maaoui M.
    Mol Biol Rep; 2022 May 28; 49(5):3823-3837. PubMed ID: 35142982
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  • 14. Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene.
    Kovac M, Tomka M, Ciernikova S, Stevurkova V, Valachova A, Zajac V.
    Clin Genet; 2006 Feb 28; 69(2):183-6. PubMed ID: 16433700
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  • 15. Familial adenomatous polyposis.
    Half E, Bercovich D, Rozen P.
    Orphanet J Rare Dis; 2009 Oct 12; 4():22. PubMed ID: 19822006
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  • 18. Clinical and molecular features of attenuated adenomatous polyposis in northern Italy.
    de Leon MP, Urso ED, Pucciarelli S, Agostini M, Nitti D, Roncucci L, Benatti P, Pedroni M, Kaleci S, Balsamo A, Laudi C, Di Gregorio C, Viel A, Rossi G, Venesio T.
    Tech Coloproctol; 2013 Feb 12; 17(1):79-87. PubMed ID: 22976915
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  • 20. Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP).
    Ghadamyari F, Heidari MM, Zeinali S, Khatami M, Merat S, Bagherian H, Rejali L, Ghasemi F.
    J Clin Lab Anal; 2021 May 12; 35(5):e23768. PubMed ID: 33769591
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