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    Results: 1 to 20 of 38

    1.

    Early-onset breast cancer in a Lebanese family with Lynch syndrome due to MSH2 gene mutation.

    Akoum R, Ghaoui A, Brihi E, Ghabash M, Hajjar N.

    Hered Cancer Clin Pract. 2009 May 28;7(1):10.

    PMID:
    19476642
    [PubMed]
    Free PMC Article
    2.

    Breast cancer in an MSH2 gene mutation carrier.

    Westenend PJ, Schütte R, Hoogmans MM, Wagner A, Dinjens WN.

    Hum Pathol. 2005 Dec;36(12):1322-6.

    PMID:
    16311127
    [PubMed - indexed for MEDLINE]
    3.

    Penetrance of colorectal cancer among MLH1/MSH2 carriers participating in the colorectal cancer familial registry in Ontario.

    Choi YH, Cotterchio M, McKeown-Eyssen G, Neerav M, Bapat B, Boyd K, Gallinger S, McLaughlin J, Aronson M, Briollais L.

    Hered Cancer Clin Pract. 2009 Aug 23;7(1):14.

    PMID:
    19698169
    [PubMed]
    Free PMC Article
    4.

    High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families.

    Chong G, Jarry J, Marcus V, Thiffault I, Winocour S, Monczak Y, Drouin R, Latreille J, Australie K, Bapat B, Gordon PH, Giguère Y, Gologan A, Galiatsatos P, Jass JR, Wong N, Zaor S, Palma L, Kasprzak L, Tischkowitz M, Foulkes WD.

    Hum Mutat. 2009 Aug;30(8):E797-812.

    PMID:
    19459153
    [PubMed - indexed for MEDLINE]
    5.

    A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers.

    Pouchet CJ, Wong N, Chong G, Sheehan MJ, Schneider G, Rosen-Sheidley B, Foulkes W, Tischkowitz M.

    Ann Oncol. 2009 Apr;20(4):681-8. Epub 2009 Jan 22.

    PMID:
    19164453
    [PubMed - indexed for MEDLINE]
    Free Article
    6.

    Mismatch repair genes in Lynch syndrome: a review.

    Silva FC, Valentin MD, Ferreira Fde O, Carraro DM, Rossi BM.

    Sao Paulo Med J. 2009 Jan;127(1):46-51. Review.

    PMID:
    19466295
    [PubMed - indexed for MEDLINE]
    Free Article
    7.

    Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.

    Järvinen HJ, Renkonen-Sinisalo L, Aktán-Collán K, Peltomäki P, Aaltonen LA, Mecklin JP.

    J Clin Oncol. 2009 Oct 1;27(28):4793-7. Epub 2009 Aug 31.

    PMID:
    19720893
    [PubMed - indexed for MEDLINE]
    8.

    Prospective evaluation of DNA mismatch repair protein expression in primary endometrial cancer.

    Backes FJ, Leon ME, Ivanov I, Suarez A, Frankel WL, Hampel H, Fowler JM, Copeland LJ, O'Malley DM, Cohn DE.

    Gynecol Oncol. 2009 Sep;114(3):486-90. Epub 2009 Jun 10.

    PMID:
    19515405
    [PubMed - indexed for MEDLINE]
    9.

    Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer.

    Plevova P, Walczyskova S, Jeziskova I, Jurckova N, Krepelova A, Puchmajerova A, Pavlikova K, Foretova L, Zapletalova J, Silhanova E.

    Neoplasma. 2009;56(6):500-7.

    PMID:
    19728758
    [PubMed - indexed for MEDLINE]
    10.

    Solitary subungual keratoacanthoma arising in an MSH2 germline mutation carrier: confirmation of a relationship by immunohistochemical analysis.

    Stoebner PE, Fabre C, Delfour C, Joujoux JM, Roger P, Dandurand M, Meunier L.

    Dermatology. 2009;219(2):174-8. Epub 2009 Jul 14.

    PMID:
    19602866
    [PubMed - indexed for MEDLINE]
    11.

    Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients.

    Resnick K, Straughn JM Jr, Backes F, Hampel H, Matthews KS, Cohn DE.

    Obstet Gynecol. 2009 Sep;114(3):530-6.

    PMID:
    19701031
    [PubMed - indexed for MEDLINE]
    12.

    Alport syndrome. Molecular genetic aspects.

    Hertz JM.

    Dan Med Bull. 2009 Aug;56(3):105-52.

    PMID:
    19728970
    [PubMed - indexed for MEDLINE]
    13.

    [Familial colorectal cancer type X: clinical, pathological and molecular characterization].

    Ferreira S, Lage P, Sousa R, Claro I, Francisco I, Filipe B, Suspiro A, Chaves P, Rodrigues P, Albuquerque C, Nobre Leitão C.

    Acta Med Port. 2009 May-Jun;22(3):207-14. Epub 2009 Jul 15. Portuguese.

    PMID:
    19686620
    [PubMed - indexed for MEDLINE]
    Free Article
    14.

    Risk of pancreatic cancer in families with Lynch syndrome.

    Kastrinos F, Mukherjee B, Tayob N, Wang F, Sparr J, Raymond VM, Bandipalliam P, Stoffel EM, Gruber SB, Syngal S.

    JAMA. 2009 Oct 28;302(16):1790-5.

    PMID:
    19861671
    [PubMed - indexed for MEDLINE]
    15.

    Germ-line mutations in mismatch repair genes associated with prostate cancer.

    Grindedal EM, Møller P, Eeles R, Stormorken AT, Bowitz-Lothe IM, Landrø SM, Clark N, Kvåle R, Shanley S, Maehle L.

    Cancer Epidemiol Biomarkers Prev. 2009 Sep;18(9):2460-7. Epub 2009 Sep 1.

    PMID:
    19723918
    [PubMed - indexed for MEDLINE]
    Free Article
    16.

    Four novel germline mutations in the MLH1 and PMS2 mismatch repair genes in patients with hereditary nonpolyposis colorectal cancer.

    Montazer Haghighi M, Radpour R, Aghajani K, Zali N, Molaei M, Zali MR.

    Int J Colorectal Dis. 2009 Aug;24(8):885-93. Epub 2009 May 29.

    PMID:
    19479271
    [PubMed - indexed for MEDLINE]
    17.

    A new mutation in the hMSH2 gene in a Spanish Lynch syndrome family.

    Zárate R, Patiño-García A, Sola J, García-Foncillas J.

    Clin Transl Oncol. 2010 Dec;12(12):849-51.

    PMID:
    21156417
    [PubMed - in process]
    18.

    Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.

    Ferreira AM, Westers H, Sousa S, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, Reuvekamp PT, Seruca R, Kleibeuker JH, Hollema H, Sijmons RH, Hofstra RM.

    J Pathol. 2009 Sep;219(1):96-102.

    PMID:
    19521971
    [PubMed - indexed for MEDLINE]
    19.

    The accuracy of risks for cancer in Lynch Syndrome.

    Hawkins AK.

    Clin Genet. 2011 Aug 24. doi: 10.1111/j.1399-0004.2011.01767.x. [Epub ahead of print]

    PMID:
    21883164
    [PubMed - as supplied by publisher]
    20.

    Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.

    Ronan SM, Tran-Viet KN, Burner EL, Metlapally R, Toth CA, Young TL.

    Arch Ophthalmol. 2009 Nov;127(11):1511-9.

    PMID:
    19901218
    [PubMed - indexed for MEDLINE]
    Free Article

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