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854 results

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Page 1
Hereditary colorectal cancer.
Lynch HT, de la Chapelle A. Lynch HT, et al. N Engl J Med. 2003 Mar 6;348(10):919-32. doi: 10.1056/NEJMra012242. N Engl J Med. 2003. PMID: 12621137 Free article. Review. No abstract available.
TGFBR1*6A may contribute to hereditary colorectal cancer.
Bian Y, Caldes T, Wijnen J, Franken P, Vasen H, Kaklamani V, Nafa K, Peterlongo P, Ellis N, Baron JA, Burn J, Moeslein G, Morrison PJ, Chen Y, Ahsan H, Watson P, Lynch HT, de la Chapelle A, Fodde R, Pasche B. Bian Y, et al. Among authors: lynch ht. J Clin Oncol. 2005 May 1;23(13):3074-8. doi: 10.1200/JCO.2005.00.281. J Clin Oncol. 2005. PMID: 15860866
PMS2 monoallelic mutation carriers: the known unknown.
Goodenberger ML, Thomas BC, Riegert-Johnson D, Boland CR, Plon SE, Clendenning M, Win AK, Senter L, Lipkin SM, Stadler ZK, Macrae FA, Lynch HT, Weitzel JN, de la Chapelle A, Syngal S, Lynch P, Parry S, Jenkins MA, Gallinger S, Holter S, Aronson M, Newcomb PA, Burnett T, Le Marchand L, Pichurin P, Hampel H, Terdiman JP, Lu KH, Thibodeau S, Lindor NM. Goodenberger ML, et al. Among authors: lynch ht, lynch p. Genet Med. 2016 Jan;18(1):13-9. doi: 10.1038/gim.2015.27. Epub 2015 Apr 9. Genet Med. 2016. PMID: 25856668 Free PMC article. Review.
Methylated SEPTIN9 plasma test for colorectal cancer detection may be applicable to Lynch syndrome.
Hitchins MP, Vogelaar IP, Brennan K, Haraldsdottir S, Zhou N, Martin B, Alvarez R, Yuan X, Kim S, Guindi M, Hendifar AE, Kalady MF, DeVecchio J, Church JM, de la Chapelle A, Hampel H, Pearlman R, Christensen M, Snyder C, Lanspa SJ, Haile RW, Lynch HT. Hitchins MP, et al. Among authors: lynch ht. BMJ Open Gastroenterol. 2019 May 28;6(1):e000299. doi: 10.1136/bmjgast-2019-000299. eCollection 2019. BMJ Open Gastroenterol. 2019. PMID: 31275589 Free PMC article.
Immunology and the Lynch syndrome.
Lynch HT, Drescher KM, de la Chapelle A. Lynch HT, et al. Gastroenterology. 2008 Apr;134(4):1246-9. doi: 10.1053/j.gastro.2008.02.008. Gastroenterology. 2008. PMID: 18395102 Free PMC article. No abstract available.
Origins and prevalence of the American Founder Mutation of MSH2.
Clendenning M, Baze ME, Sun S, Walsh K, Liyanarachchi S, Fix D, Schunemann V, Comeras I, Deacon M, Lynch JF, Gong G, Thomas BC, Thibodeau SN, Lynch HT, Hampel H, de la Chapelle A. Clendenning M, et al. Among authors: lynch jf, lynch ht. Cancer Res. 2008 Apr 1;68(7):2145-53. doi: 10.1158/0008-5472.CAN-07-6599. Cancer Res. 2008. PMID: 18381419
854 results