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Journal Abstract Search

545 related items for PubMed ID: 7661930

  • 1. The molecular basis of Turcot's syndrome.
    Hamilton SR, Liu B, Parsons RE, Papadopoulos N, Jen J, Powell SM, Krush AJ, Berk T, Cohen Z, Tetu B.
    N Engl J Med; 1995 Mar 30; 332(13):839-47. PubMed ID: 7661930
    [Abstract] [Full Text] [Related]

  • 2. Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.
    Heinimann K, Thompson A, Locher A, Furlanetto T, Bader E, Wolf A, Meier R, Walter K, Bauerfeind P, Marra G, Müller H, Foernzler D, Dobbie Z.
    Cancer Res; 2001 Oct 15; 61(20):7616-22. PubMed ID: 11606402
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  • 3. Survival of patients with Turcot's syndrome and glioblastoma.
    Merlo A, Rochlitz C, Scott R.
    N Engl J Med; 1996 Mar 14; 334(11):736-7. PubMed ID: 8594446
    [No Abstract] [Full Text] [Related]

  • 4. [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 Mar 14; 145(6):475-9. PubMed ID: 16836001
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  • 6. Deletion analysis of the adenomatous polyposis coli and PTCH gene loci in patients with sporadic and nevoid basal cell carcinoma syndrome-associated medulloblastoma.
    Vortmeyer AO, Stavrou T, Selby D, Li G, Weil RJ, Park WS, Moon YW, Chandra R, Goldstein AM, Zhuang Z.
    Cancer; 1999 Jun 15; 85(12):2662-7. PubMed ID: 10375116
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  • 8. [Muir-Torre syndrome and familial colorectal cancer: 2 families with molecular genetic analysis].
    Doré MX, Dieumegard B, Grandjouan S, Avril MF, Martinet C, Ducreux M, Lasser P, Bressac-de Paillerets B.
    Ann Dermatol Venereol; 1999 Jun 15; 126(8-9):582-6. PubMed ID: 10530344
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  • 10. 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 15; 71(5):427-33. PubMed ID: 17489848
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  • 12. Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization.
    Kanter-Smoler G, Björk J, Fritzell K, Engwall Y, Hallberg B, Karlsson G, Grönberg H, Karlsson P, Wallgren A, Wahlström J, Hultcrantz R, Nordling M.
    Clin Gastroenterol Hepatol; 2006 Apr 15; 4(4):499-506. PubMed ID: 16616356
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  • 13. Turcot syndrome (glioma polyposis): a case report.
    Sarin S, Bernath A.
    South Med J; 2008 Dec 15; 101(12):1273-4. PubMed ID: 19005436
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  • 14. Genetic testing for germline mutations of the APC gene in patients with apparently sporadic desmoid tumors but a family history of colorectal carcinoma.
    Brueckl WM, Ballhausen WG, Förtsch T, Günther K, Fiedler W, Gentner B, Croner R, Boxberger F, Kirchner T, Hahn EG, Hohenberger W, Wein A.
    Dis Colon Rectum; 2005 Jun 15; 48(6):1275-81. PubMed ID: 15793634
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  • 16. Is prophylactic colectomy indicated in patients with MYH-associated polyposis?
    Leite JS, Isidro G, Martins M, Regateiro F, Albuquerque O, Amaro P, Romãozinho JM, Boavida G, Castro-Sousa F.
    Colorectal Dis; 2005 Jul 15; 7(4):327-31. PubMed ID: 15932553
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  • 18. 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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  • 19. The APC gene in Turcot's syndrome.
    Rutz HP, Kikuchi T.
    N Engl J Med; 1995 Aug 24; 333(8):524. PubMed ID: 7623895
    [No Abstract] [Full Text] [Related]

  • 20. Implication of adenomatous polyposis coli and MUTYH mutations in familial colorectal polyposis.
    De Rosa M, Galatola M, Borriello S, Duraturo F, Masone S, Izzo P.
    Dis Colon Rectum; 2009 Feb 24; 52(2):268-74. PubMed ID: 19279422
    [Abstract] [Full Text] [Related]

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