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Journal Abstract Search

485 related items for PubMed ID: 12172928

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  • 7. Investigation of APC mutations in a Turkish familial adenomatous polyposis family by heterodublex analysis.
    Tunca B, Menigatti M, Benatti P, Egeli U, Cecener G, Pedroni M, Scarselli A, Borghi F, Sala E, Yilmazlar T, Zorluoglu A, Yerci O, de Leon MP.
    Dis Colon Rectum; 2005 Mar; 48(3):567-71. PubMed ID: 15719192
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  • 8. Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.
    Li G, Tamura K, Yamamoto Y, Sashio H, Utsunomiya J, Yamamura T, Shimoyama T, Furuyama J.
    J Exp Clin Cancer Res; 1999 Dec; 18(4):519-29. PubMed ID: 10746979
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  • 9. 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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  • 11. Molecular analysis of the APC and MYH genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations.
    Vandrovcová J, Stekrová J, Kebrdlová V, Kohoutová M.
    Hum Mutat; 2004 Apr; 23(4):397. PubMed ID: 15024739
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  • 13. Mutation analysis of the adenomatous polyposis coli (APC) gene in northwest Spanish patients with familial adenomatous polyposis (FAP) and sporadic colorectal cancer.
    Ruiz-Ponte C, Vega A, Carracedo A, Barros F.
    Hum Mutat; 2001 Oct; 18(4):355. PubMed ID: 11668620
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  • 15. Novel germline mutations in the APC gene of Cypriot patients with familial and sporadic adenomatous polyposis.
    Hadjisavvas A, Papasavva T, Loizidou M, Malas S, Potamitis G, Christodoulou C, Pavlides G, Papamichael D, Klonis C, Nasioulas G, Anastasiadou V, Kyriacou K.
    Clin Genet; 2006 May; 69(5):404-9. PubMed ID: 16650078
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  • 16. The mutation spectrum of the APC gene in Turkish patients with familial adenomatous polyposis.
    Tunca B, Cecener G, Egeli U, Zorluoglu A, Yilmazlar T.
    Dis Colon Rectum; 2007 Nov; 50(11):1899-904. PubMed ID: 17882487
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  • 17. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
    Valanzano R, Cama A, Volpe R, Curia MC, Mencucci R, Palmirotta R, Battista P, Ficari F, Mariani-Costantini R, Tonelli F.
    Cancer; 1996 Dec 01; 78(11):2400-10. PubMed ID: 8941012
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  • 18. Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients.
    Mihalatos M, Apessos A, Dauwerse H, Velissariou V, Psychias A, Koliopanos A, Petropoulos K, Triantafillidis JK, Danielidis I, Fountzilas G, Agnantis NJ, Nasioulas G.
    BMC Cancer; 2005 Apr 15; 5():40. PubMed ID: 15833136
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  • 19. Identification of APC exon 15 mutations in families suspected of familial adenomatous polyposis (FAP).
    Kirchhoff T, Zajac V, Krizan P, Repiská V, Stevurková V, Friedl W.
    Folia Biol (Praha); 1997 Apr 15; 43(5):203-9. PubMed ID: 9595262
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  • 20. Adenomatous polyposis families that screen APC mutation-negative by conventional methods are genetically heterogeneous.
    Renkonen ET, Nieminen P, Abdel-Rahman WM, Moisio AL, Järvelä I, Arte S, Järvinen HJ, Peltomäki P.
    J Clin Oncol; 2005 Aug 20; 23(24):5651-9. PubMed ID: 16110024
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