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Journal Abstract Search

304 related items for PubMed ID: 20924072

  • 1. 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; 22(4):903-909. PubMed ID: 20924072
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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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  • 4. Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?
    Gómez-Fernández N, Castellví-Bel S, Fernández-Rozadilla C, Balaguer F, Muñoz J, Madrigal I, Milà M, Graña B, Vega A, Castells A, Carracedo A, Ruiz-Ponte C.
    BMC Med Genet; 2009 Jun 16; 10():57. PubMed ID: 19531215
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  • 6. 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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  • 7. 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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  • 9. 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 05; 20(12):777-785. PubMed ID: 27705013
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  • 11. APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
    Filipe B, Baltazar C, Albuquerque C, Fragoso S, Lage P, Vitoriano I, Mão de Ferro S, Claro I, Rodrigues P, Fidalgo P, Chaves P, Cravo M, Nobre Leitão C.
    Clin Genet; 2009 Sep 05; 76(3):242-55. PubMed ID: 19793053
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  • 16. 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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  • 18. Synonymous mutation adenomatous polyposis coliΔ486s affects exon splicing and may predispose patients to adenomatous polyposis coli/mutY DNA glycosylase mutation‑negative familial adenomatous polyposis.
    Liu WQ, Dong J, Peng YX, Li WL, Yang J.
    Mol Med Rep; 2018 Dec 15; 18(6):4931-4939. PubMed ID: 30272267
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  • 19. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.
    Araujo LF, Molfetta GA, Vincenzi OC, Huber J, Teixeira LA, Ferraz VE, Silva WA.
    Int J Biol Markers; 2019 Mar 15; 34(1):80-89. PubMed ID: 30852976
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  • 20. Mutation Spectrum of Familial Adenomatous Polyposis Patients in Turkish Population: Identification of 3 Novel APC Mutations.
    Arslan Ateş E, Alavanda C, Demir Ş, Keklikkıran Ç, Attaallah W, Özdoğan OC, Güney Aİ.
    Turk J Gastroenterol; 2022 Feb 15; 33(2):81-87. PubMed ID: 35238777
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