| 1 | HNPCC5, MSH6
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| Characterization of two Ashkenazi Jewish founder mutations in MSH6 gene causing Lynch syndrome.
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| Raskin L, Schwenter F, Freytsis M, Tischkowitz M, Wong N, Chong G, Narod S, Levine D, Bogomolniy F, Aronson M, Thibodeau S, Hunt K, Rennert G, Gallinger S, Gruber S, Foulkes W.
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| Clin Genet 79(6):512-522. doi: 10.1111/j.1399-0004.2010.01594.x. Epub 2010 Dec 14.
2011
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| 2 | MSH6, HNPCC5, MUTYH
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| No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
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| Steinke V, Rahner N, Morak M, Keller G, Schackert HK, Grgens H, Schmiegel W, Royer-Pokora B, Dietmaier W, Kloor M, Engel C, Propping P, Aretz S; for The German HNPCC Consortium.
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| Eur J Hum Genet 16(5):587-592. Epub 2008 Feb 27. 2008
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| 3 | HNPCC1, HNPCC2, HNPCC3, HNPCC4, HNPCC5, HNPCC6, HNPCC7, MLH1, MSH2, MSH6, PMS2
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| Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer).
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| Vasen HF, Moslein G, Alonso A, Bernstein I, Bertario L, Blanco I, Burn J, Capella G, Engel C, Frayling I, Friedl W, Hes FJ, Hodgson S, Mecklin JP, Moller P, Nagengast F, Parc Y, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Wijnen J.
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| J Med Genet 44(6):353-62. Epub 2007 Feb 27. 2007
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| 4 | HNPCC1, HNPCC2, HNPCC3, HNPCC4, HNPCC5, HNPCC6, HNPCC7
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| Constitutive deficiency in DNA mismatch repair: is it time for Lynch III?
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| Felton K, Gilchrist D, Andrew S.
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| Clin Genet 71(6):499-500. 2007
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| 5 | HNPCC1, HNPCC2, HNPCC3, HNPCC4, HNPCC5, HNPCC6, HNPCC7
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| Constitutive deficiency in DNA mismatch repair.
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| Felton K, Gilchrist D, Andrew S.
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| Clin Genet 71(6):483-98. 2007
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| 6 | MSH2, MLH1, MSH6, PMS2, HNPCC1, HNPCC2, HNPCC5, HNPCC4
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| Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC).
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| van der Klift H, Wijnen J, Wagner A, Verkuilen P, Tops C, Otway R, Kohonen-Corish M, Vasen H, Oliani C, Barana D, Moller P, Delozier-Blanchet C, Hutter P, Foulkes W, Lynch H, Burn J, Moslein G, Fodde R.
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| Genes Chromosomes Cancer 44(2):123-38. 2005
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| 7 | MSH2, MLH1, MSH6, PMS2, MLH3, PMS1, HNPCC1, HNPCC2, HNPCC5, HNPCC4, HNPCC3, HNPCC6
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| Lynch syndrome genes.
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| Peltomaki P.
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| Fam Cancer 4(3):227-32. Review. 2005
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| 8 | HNPCC1, HNPCC2, HNPCC3, HNPCC4, HNPCC5, HNPCC6, HNPCC7, MLH1, MSH2, MSH6, PMS2
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| Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.
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| Peltomaki P, Vasen H.
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| Dis Markers 20(4-5):269-76. Review. 2004
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| 9 | HNPCC5, MSH6
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| Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree.
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| Wagner A, Hendriks Y, Meijers-Heijboer EJ, de Leeuw WJ, Morreau H, Hofstra R, Tops C, Bik E, Brocker-Vriends AH, van Der Meer C, Lindhout D, Vasen HF, Breuning MH, Cornelisse CJ, van Krimpen C, Niermeijer MF, Zwinderman AH, Wijnen J, Fodde R.
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| J Med Genet 38(5):318-22. 2001
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| 10 | HNPCC1, HNPCC2, HNPCC3, HNPCC4, HNPCC5, HNPCC6, HNPCC7
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| Deficient DNA mismatch repair: a common etiologic factor for colon cancer.
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| Peltomaki P.
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| Hum Mol Genet 10(7):735-40. Review. 2001
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| 11 | HNPCC5, MSH6
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| hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden.
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| Planck M, Koul A, Fernebro E, Borg A, Kristoffersson U, Olsson H, Wenngren E, Mangell P, Nilbert M.
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| Int J Cancer 83(2):197-202 1999
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| 12 | MSH6, HNPCC5
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| Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer.
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| Miyaki M, Konishi M, Tanaka K, Kikuchi-Yanoshita R, Muraoka M, Yasuno M, Igari T, Koike M, Chiba M, Mori T.
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| Nat Genet 17(3):271-2. 1997
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| 13 | MSH6, HNPCC2, HNPCC5, MSH3
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| Mutation of hMSH3 and hMSH6 mismatch repair genes in genetically unstable human colorectal and gastric carcinomas.
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| Yin J, Kong D, Wang S, Zou TT, Souza RF, Smolinski KN, Lynch PM, Hamilton SR, Sugimura H, Powell SM, Young J, Abraham JM, Meltzer SJ.
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| Hum Mutat 10(6):474-8. 1997
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