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Journal Abstract Search

377 related items for PubMed ID: 30272267

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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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  • 3. 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; 35(5):e23768. PubMed ID: 33769591
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  • 4. 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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  • 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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  • 10. 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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  • 11. A novel pathogenic large germline deletion in adenomatous polyposis coli gene in a Chinese family with familial adenomatous polyposis.
    Zhang Z, Liang S, Huang H, Wang D, Zhang X, Wu J, Chen H, Wang Y, Rong T, Zhou Y, Banerjee S.
    Oncotarget; 2016 Aug 02; 7(31):50392-50400. PubMed ID: 27391059
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