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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2006 | 1 |
2011 | 1 |
2012 | 2 |
2013 | 1 |
2015 | 1 |
2024 | 0 |
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Page 1
Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity.
Mol Carcinog. 2015 Jul;54(7):513-22. doi: 10.1002/mc.22116. Epub 2013 Dec 2.
Mol Carcinog. 2015.
PMID: 24302565
Free PMC article.
Cancer risk in 348 French MSH2 or MLH1 gene carriers.
Parc Y, Boisson C, Thomas G, Olschwang S.
Parc Y, et al.
J Med Genet. 2003 Mar;40(3):208-13. doi: 10.1136/jmg.40.3.208.
J Med Genet. 2003.
PMID: 12624141
Free PMC article.
No abstract available.
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Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer.
Barnetson RA, Tenesa A, Farrington SM, Nicholl ID, Cetnarskyj R, Porteous ME, Campbell H, Dunlop MG.
Barnetson RA, et al.
N Engl J Med. 2006 Jun 29;354(26):2751-63. doi: 10.1056/NEJMoa053493.
N Engl J Med. 2006.
PMID: 16807412
Free article.
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Screening for Lynch syndrome in colorectal cancer: are we doing enough?
Canard G, Lefevre JH, Colas C, Coulet F, Svrcek M, Lascols O, Hamelin R, Shields C, Duval A, Fléjou JF, Soubrier F, Tiret E, Parc Y.
Canard G, et al.
Ann Surg Oncol. 2012 Mar;19(3):809-16. doi: 10.1245/s10434-011-2014-7. Epub 2011 Aug 31.
Ann Surg Oncol. 2012.
PMID: 21879275
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Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome.
van Lier MG, Leenen CH, Wagner A, Ramsoekh D, Dubbink HJ, van den Ouweland AM, Westenend PJ, de Graaf EJ, Wolters LM, Vrijland WW, Kuipers EJ, van Leerdam ME, Steyerberg EW, Dinjens WN; LIMO Study Group.
van Lier MG, et al.
J Pathol. 2012 Apr;226(5):764-74. doi: 10.1002/path.3963. Epub 2012 Jan 17.
J Pathol. 2012.
PMID: 22081473
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