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Items: 10


Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients.

Masson AL, Talseth-Palmer BA, Evans TJ, McElduff P, Spigelman AD, Hannan GN, Scott RJ.

Meta Gene. 2015 Dec 24;7:95-104. doi: 10.1016/j.mgene.2015.12.005. eCollection 2016 Feb.


Colorectal cancer in Chinese patients: current and emerging treatment options.

Li L, Ma BB.

Onco Targets Ther. 2014 Oct 4;7:1817-28. doi: 10.2147/OTT.S48409. eCollection 2014. Review.


Expanding the genetic basis of copy number variation in familial breast cancer.

Masson AL, Talseth-Palmer BA, Evans TJ, Grice DM, Hannan GN, Scott RJ.

Hered Cancer Clin Pract. 2014 May 24;12(1):15. doi: 10.1186/1897-4287-12-15. eCollection 2014.


Expression sensitivity analysis of human disease related genes.

Ma LX, Wang YJ, Wang JF, Li X, Hao P.

Biomed Res Int. 2013;2013:637424. doi: 10.1155/2013/637424. Epub 2013 Nov 24.


Alterations of copy number of methylation pattern in mismatch repair genes by methylation specific-multiplex ligation-dependent probe amplification in cases of colon cancer.

Onrat S, Ceken I, Ellidokuz E, Kupelio─člu A.

Balkan J Med Genet. 2011 Dec;14(2):25-34. doi: 10.2478/v10034-011-0044-x.


Hereditary Colorectal Cancer Syndromes in Hong Kong: a Registry's Perspective.

Ho JW, Wei R, Chan EM.

Hered Cancer Clin Pract. 2005 Oct 15;3(4):147-54. doi: 10.1186/1897-4287-3-4-147.


Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers.

Zavodna K, Krivulcik T, Bujalkova MG, Slamka T, Martinicky D, Ilencikova D, Bartosova Z.

BMC Cancer. 2009 Nov 20;9:405. doi: 10.1186/1471-2407-9-405.


Copy number variations and cancer.

Shlien A, Malkin D.

Genome Med. 2009 Jun 16;1(6):62. doi: 10.1186/gm62.


MSH2 c.1452-1455delAATG is a founder mutation and an important cause of hereditary nonpolyposis colorectal cancer in the southern Chinese population.

Chan TL, Chan YW, Ho JW, Chan C, Chan AS, Chan E, Lam PW, Tse CW, Lee KC, Lau CW, Gwi E, Leung SY, Yuen ST.

Am J Hum Genet. 2004 May;74(5):1035-42. Epub 2004 Mar 23.


The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CM, Bonner JD, Nafa K, Walsh T, Marcus V, Tomsho L, Gebert J, Macrae FA, Gaff CL, Paillerets BB, Gregersen PK, Weitzel JN, Gordon PH, MacNamara E, King MC, Hampel H, De La Chapelle A, Boyd J, Offit K, Rennert G, Chong G, Ellis NA.

Am J Hum Genet. 2002 Dec;71(6):1395-412. Epub 2002 Nov 26.

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