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Journal Abstract Search

283 related items for PubMed ID: 16201232

  • 21. [Genetic diagnosis of familial adenomatous polyposis: detection of APC gene mutations based on an in vitro synthetized protein].
    Albuquerque C, Fidalgo P, Chagas C, Suspiro A, Cravo M, Ramalho E, Leitão CN, Mira FC.
    Acta Med Port; 1998 Jan; 11(1):25-32. PubMed ID: 9580364
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  • 22. Screening for mutations of the APC gene in 66 Italian familial adenomatous polyposis patients: evidence for phenotypic differences in cases with and without identified mutation.
    Giarola M, Stagi L, Presciuttini S, Mondini P, Radice MT, Sala P, Pierotti MA, Bertario L, Radice P.
    Hum Mutat; 1999 Jan; 13(2):116-23. PubMed ID: 10094547
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  • 23. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?
    Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T.
    Pediatr Blood Cancer; 2006 Nov; 47(6):811-8. PubMed ID: 16317745
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  • 24. APC gene mutations and colorectal adenomatosis in familial adenomatous polyposis.
    Ficari F, Cama A, Valanzano R, Curia MC, Palmirotta R, Aceto G, Esposito DL, Crognale S, Lombardi A, Messerini L, Mariani-Costantini R, Tonelli F, Battista P.
    Br J Cancer; 2000 Jan; 82(2):348-53. PubMed ID: 10646887
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  • 25. Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition.
    Wallis YL, Morton DG, McKeown CM, Macdonald F.
    J Med Genet; 1999 Jan; 36(1):14-20. PubMed ID: 9950360
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  • 26. APC germline mutations identified in Czech patients with familial adenomatous polyposis.
    Kohoutová M, Stekrová J, Jirásek V, Kapras J.
    Hum Mutat; 2002 Apr; 19(4):460-1. PubMed ID: 11933206
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  • 27. Correlation between the location of germ-line mutations in the APC gene and the number of colorectal polyps in familial adenomatous polyposis patients.
    Nagase H, Miyoshi Y, Horii A, Aoki T, Ogawa M, Utsunomiya J, Baba S, Sasazuki T, Nakamura Y.
    Cancer Res; 1992 Jul 15; 52(14):4055-7. PubMed ID: 1319838
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  • 31. Characterization of APC exon 15 germ-line mutation in FAP family with severe phenotype showing extracolonic symptoms.
    Kirchhoff T, Kulcsár L, Tomka M, Stevurková V, Zajac V.
    Neoplasma; 1999 Jul 15; 46(5):290-4. PubMed ID: 10665844
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  • 32. [Germline mutation of adenomatous polyposis coli gene in Chinese patients with familial adenomatous polyposis].
    Wang TT, Chen SQ, Zhang XM.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr 15; 25(2):199-202. PubMed ID: 18393246
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  • 33. Genome-wide scan identifies a copy number variable region at 3q26 that regulates PPM1L in APC mutation-negative familial colorectal cancer patients.
    Thean LF, Loi C, Ho KS, Koh PK, Eu KW, Cheah PY.
    Genes Chromosomes Cancer; 2010 Feb 15; 49(2):99-106. PubMed ID: 19847890
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  • 34. Promoter hypermethylation leads to decreased APC mRNA expression in familial polyposis and sporadic colorectal tumours, but does not substitute for truncating mutations.
    Segditsas S, Sieber OM, Rowan A, Setien F, Neale K, Phillips RK, Ward R, Esteller M, Tomlinson IP.
    Exp Mol Pathol; 2008 Dec 15; 85(3):201-6. PubMed ID: 18977219
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  • 35. Molecular diagnosis of familial adenomatous polyposis.
    Powell SM, Petersen GM, Krush AJ, Booker S, Jen J, Giardiello FM, Hamilton SR, Vogelstein B, Kinzler KW.
    N Engl J Med; 1993 Dec 30; 329(27):1982-7. PubMed ID: 8247073
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  • 39. [Hereditary forms of colorectal adenomatous polyposis].
    Kohoutová M, Stekrová J, Sulová M, Zidková K, Kleibl Z, Vandrovcová J, Kebrdlová V, Kotlas J, Jirásek V.
    Cas Lek Cesk; 2006 Dec 30; 145(6):475-9. PubMed ID: 16836001
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  • 40. [Familial adenomatous polyposis syndrome (FAP): pathogenesis and molecular mechanisms].
    Friedrich A, Kullmann F.
    Med Klin (Munich); 2003 Dec 15; 98(12):776-82. PubMed ID: 14685680
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