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Results: 9

Cited In for PubMed (Select 16251890)


Applicability of next generation sequencing technology in microsatellite instability testing.

Gan C, Love C, Beshay V, Macrae F, Fox S, Waring P, Taylor G.

Genes (Basel). 2015 Feb 12;6(1):46-59. doi: 10.3390/genes6010046.


Poly(A) motif prediction using spectral latent features from human DNA sequences.

Xie B, Jankovic BR, Bajic VB, Song L, Gao X.

Bioinformatics. 2013 Jul 1;29(13):i316-25. doi: 10.1093/bioinformatics/btt218.


MLPAstats: an R GUI package for the integrated analysis of copy number alterations using MLPA data.

Cáceres A, Armengol L, Villatoro S, González JR.

BMC Bioinformatics. 2011 May 11;12:147. doi: 10.1186/1471-2105-12-147.


Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry.

Cicek MS, Lindor NM, Gallinger S, Bapat B, Hopper JL, Jenkins MA, Young J, Buchanan D, Walsh MD, Le Marchand L, Burnett T, Newcomb PA, Grady WM, Haile RW, Casey G, Plummer SJ, Krumroy LA, Baron JA, Thibodeau SN.

J Mol Diagn. 2011 May;13(3):271-81. doi: 10.1016/j.jmoldx.2010.12.004.


An optimized pentaplex PCR for detecting DNA mismatch repair-deficient colorectal cancers.

Goel A, Nagasaka T, Hamelin R, Boland CR.

PLoS One. 2010 Feb 24;5(2):e9393. doi: 10.1371/journal.pone.0009393. Erratum in: PLoS One. 2010;5(3). doi: 10.1371/annotation/572bb6d3-0315-40b1-a6d7-ce818809b5ea.


Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome.

Giunti L, Cetica V, Ricci U, Giglio S, Sardi I, Paglierani M, Andreucci E, Sanzo M, Forni M, Buccoliero AM, Genitori L, Genuardi M.

Eur J Hum Genet. 2009 Jul;17(7):919-27. doi: 10.1038/ejhg.2008.271. Epub 2009 Jan 21.


EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.

Palomaki GE, McClain MR, Melillo S, Hampel HL, Thibodeau SN.

Genet Med. 2009 Jan;11(1):42-65. doi: 10.1097/GIM.0b013e31818fa2db. Review. No abstract available.


Multiplex ligation-dependent probe amplification identification of whole exon and single nucleotide deletions in the CFTR gene of Hispanic individuals with cystic fibrosis.

Schrijver I, Rappahahn K, Pique L, Kharrazi M, Wong LJ.

J Mol Diagn. 2008 Jul;10(4):368-75. doi: 10.2353/jmoldx.2008.080004. Epub 2008 Jun 13.


Probe-specific mixed-model approach to detect copy number differences using multiplex ligation-dependent probe amplification (MLPA).

González JR, Carrasco JL, Armengol L, Villatoro S, Jover L, Yasui Y, Estivill X.

BMC Bioinformatics. 2008 Jun 4;9:261. doi: 10.1186/1471-2105-9-261.

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