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Journal Abstract Search

273 related items for PubMed ID: 22167527

  • 21. Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome.
    Zighelboim I, Powell MA, Babb SA, Whelan AJ, Schmidt AP, Clendenning M, Senter L, Thibodeau SN, de la Chapelle A, Goodfellow PJ.
    Fam Cancer; 2009; 8(4):501-4. PubMed ID: 19672700
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  • 22. Universal screening for Lynch syndrome in endometrial cancers: frequency of germline mutations and identification of patients with Lynch-like syndrome.
    Dillon JL, Gonzalez JL, DeMars L, Bloch KJ, Tafe LJ.
    Hum Pathol; 2017 Dec; 70():121-128. PubMed ID: 29107668
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  • 26. Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity.
    Baris HN, Barnes-Kedar I, Toledano H, Halpern M, Hershkovitz D, Lossos A, Lerer I, Peretz T, Kariv R, Cohen S, Half EE, Magal N, Drasinover V, Wimmer K, Goldberg Y, Bercovich D, Levi Z.
    Pediatr Blood Cancer; 2016 Mar; 63(3):418-27. PubMed ID: 26544533
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  • 27. Lynch syndrome-associated colorectal carcinoma: frequent involvement of the left colon and rectum and late-onset presentation supports a universal screening approach.
    Hartman DJ, Brand RE, Hu H, Bahary N, Dudley B, Chiosea SI, Nikiforova MN, Pai RK.
    Hum Pathol; 2013 Nov; 44(11):2518-28. PubMed ID: 24034859
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  • 28. Screening to detect Lynch syndrome and prevent hereditary cancers in relatives.
    Haddow JE, Palomaki GE.
    J Med Screen; 2011 Nov; 18(4):167-8. PubMed ID: 22184732
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  • 31. Hereditary non-polyposis colorectal cancer/Lynch syndrome in three dimensions.
    Kravochuck SE, Church JM.
    ANZ J Surg; 2017 Dec; 87(12):1006-1010. PubMed ID: 26990828
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  • 32. Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.
    Case AS, Zighelboim I, Mutch DG, Babb SA, Schmidt AP, Whelan AJ, Thibodeau SN, Goodfellow PJ.
    Gynecol Oncol; 2008 Feb; 108(2):438-44. PubMed ID: 18022218
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  • 34. Recommendations from the EGAPP Working Group: genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives.
    Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Groupegappinfo@egappreviews.org.
    Genet Med; 2009 Jan; 11(1):35-41. PubMed ID: 19125126
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  • 35. Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.
    Peltomäki P, Vasen H.
    Dis Markers; 2004 Jan; 20(4-5):269-76. PubMed ID: 15528792
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