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Journal Abstract Search

412 related items for PubMed ID: 27705013

  • 1. Colorectal Adenomatous Polyposis: Heterogeneity of Susceptibility Gene Mutations and Phenotypes in a Cohort of Italian Patients.
    Marabelli M, Molinaro V, Abou Khouzam R, Berrino E, Panero M, Balsamo A, Venesio T, Ranzani GN.
    Genet Test Mol Biomarkers; 2016 Dec; 20(12):777-785. PubMed ID: 27705013
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  • 2. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
    Papp J, Kovacs ME, Matrai Z, Orosz E, Kásler M, Børresen-Dale AL, Olah E.
    Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593
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  • 5. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort.
    Khan N, Lipsa A, Arunachal G, Ramadwar M, Sarin R.
    Sci Rep; 2017 May 22; 7(1):2214. PubMed ID: 28533537
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  • 6. Attenuated polyposis of the large bowel: a morphologic and molecular approach.
    de Leon MP, Pedroni M, Roncucci L, Domati F, Rossi G, Magnani G, Pezzi A, Fante R, Bonetti LR.
    Fam Cancer; 2017 Apr 22; 16(2):211-220. PubMed ID: 27783336
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  • 7. The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
    Claes K, Dahan K, Tejpar S, De Paepe A, Bonduelle M, Abramowicz M, Verellen C, Franchimont D, Van Cutsem E, Kartheuser A.
    Acta Gastroenterol Belg; 2011 Sep 22; 74(3):421-6. PubMed ID: 22103048
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  • 9. MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations.
    Morak M, Laner A, Bacher U, Keiling C, Holinski-Feder E.
    Clin Genet; 2010 Oct 22; 78(4):353-63. PubMed ID: 20618354
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  • 10. 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 22; 17(1):79-87. PubMed ID: 22976915
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  • 13. Mutational spectrum of the APC and MUTYH genes and genotype-phenotype correlations in Brazilian FAP, AFAP, and MAP patients.
    Torrezan GT, da Silva FC, Santos EM, Krepischi AC, Achatz MI, Aguiar S, Rossi BM, Carraro DM.
    Orphanet J Rare Dis; 2013 Apr 05; 8():54. PubMed ID: 23561487
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  • 14. 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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  • 16. Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population study.
    Rivera B, González S, Sánchez-Tomé E, Blanco I, Mercadillo F, Letón R, Benítez J, Robledo M, Capellá G, Urioste M.
    Ann Oncol; 2011 Apr 15; 22(4):903-909. PubMed ID: 20924072
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  • 19. Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.
    Cruz-Correa M, Diaz-Algorri Y, Mendez V, Vazquez PJ, Lozada ME, Freyre K, Lathroum L, Gonzalez-Pons M, Hernandez-Marrero J, Giardiello F, Rodriguez-Quilichini S.
    Fam Cancer; 2013 Sep 15; 12(3):555-62. PubMed ID: 23460355
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