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Journal Abstract Search

307 related items for PubMed ID: 31062380

  • 1. Clinical characterization and mutation spectrum in patients with familial adenomatous polyposis in China.
    Li N, Kang Q, Yang L, Zhao XJ, Xue LJ, Wang X, Li AQ, Li CG, Sheng JQ.
    J Gastroenterol Hepatol; 2019 Sep; 34(9):1497-1503. PubMed ID: 31062380
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  • 3. 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. Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients.
    Taki K, Sato Y, Nomura S, Ashihara Y, Kita M, Tajima I, Sugano K, Arai M.
    Fam Cancer; 2016 Apr 22; 15(2):261-5. PubMed ID: 26684191
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  • 13. 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 22; 71(5):427-33. PubMed ID: 17489848
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  • 14. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
    Lejeune S, Guillemot F, Triboulet JP, Cattan S, Mouton C, PAFNORD Group, Porchet N, Manouvrier S, Buisine MP.
    Hum Mutat; 2006 Oct 22; 27(10):1064. PubMed ID: 16941501
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  • 15. 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 22; 76(3):242-55. PubMed ID: 19793053
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  • 16. 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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  • 17. 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 05; 78(4):353-63. PubMed ID: 20618354
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  • 18. A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Chinese family with familial adenomatous coli.
    Jiang SS, Li JJ, Li Y, He LJ, Wang QJ, Weng DS, Pan K, Liu Q, Zhao JJ, Pan QZ, Zhang XF, Tang Y, Chen CL, Zhang HX, Xu GL, Zeng YX, Xia JC.
    Oncotarget; 2015 Sep 29; 6(29):27267-74. PubMed ID: 26311738
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  • 19. Presentation and Follow-up of Familial Adenomatous Polyposis: Differences Between APC and MUTYH Mutations.
    Bademci R, Bollo J, Ramón Y Cajal T, Martínez MC, Hernández MP, Targarona EM.
    Cir Esp (Engl Ed); 2020 Oct 29; 98(8):465-471. PubMed ID: 32505560
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  • 20. 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 29; 34(1):80-89. PubMed ID: 30852976
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