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Items: 10

1.

DNA and RNA analyses in detection of genetic predisposition to cancer.

Kurzawski G, Dymerska D, Serrano-Fernández P, Trubicka J, Masojć B, Jakubowska A, Scott RJ.

Hered Cancer Clin Pract. 2012 Dec 4;10(1):17. doi: 10.1186/1897-4287-10-17.

2.

Novel germline MSH2 mutation in lynch syndrome patient surviving multiple cancers.

Janavicius R, Elsakov P.

Hered Cancer Clin Pract. 2012 Jan 10;10(1):1. doi: 10.1186/1897-4287-10-1.

3.

A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expression.

Perera S, Li B, Tsitsikotas S, Ramyar L, Pollett A, Semotiuk K, Bapat B.

J Mol Diagn. 2010 Nov;12(6):757-64. doi: 10.2353/jmoldx.2010.090240. Epub 2010 Sep 23.

4.

The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs.

Lubiński J, Huzarski T, Kurzawski G, Suchy J, Masojć B, Mierzejewski M, Lener M, Domagała W, Chosia M, Teodorczyk U, Medrek K, Debniak T, Złowocka E, Gronwald J, Byrski T, Grabowska E, Nej K, Szymańska A, Szymańska J, Matyjasik J, Cybulski C, Jakubowska A, Górski B, Narod SA.

Hered Cancer Clin Pract. 2005 Mar 15;3(2):59-63. doi: 10.1186/1897-4287-3-2-59.

5.

Some aspects of molecular diagnostics in Lynch syndrome.

Kurzawski G.

Hered Cancer Clin Pract. 2006 Dec 15;4(4):197-205. doi: 10.1186/1897-4287-4-4-197.

6.

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients.

Dymerska D, Serrano-Fernández P, Suchy J, Pławski A, Słomski R, Kaklewski K, Scott RJ, Gronwald J, Kładny J, Byrski T, Huzarski T, Lubiński J, Kurzawski G.

J Mol Diagn. 2010 Jan;12(1):82-90. doi: 10.2353/jmoldx.2010.090063. Epub 2009 Dec 10.

7.

DNA and RNA analyses in detection of genetic predisposition to cancer.

Matyjasik J, Masojc B, Kurzawski G.

Hered Cancer Clin Pract. 2008 Jun 15;6(2):73-80. doi: 10.1186/1897-4287-6-2-73. No abstract available.

8.

Recurrent APC gene mutations in Polish FAP families.

Pławski A, Podralska M, Słomski R.

Hered Cancer Clin Pract. 2007 Dec 15;5(4):195-8. doi: 10.1186/1897-4287-5-4-195.

10.

Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain.

Ellison AR, Lofing J, Bitter GA.

Nucleic Acids Res. 2004 Oct 8;32(18):5321-38. Print 2004.

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