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Items: 3

1.

An intronic polymorphic deletion in the PTEN gene: implications for molecular diagnostic testing.

Sandell S, Schuit RJ, Bunyan DJ.

Br J Cancer. 2013 Feb 5;108(2):438-41. doi: 10.1038/bjc.2012.562. Epub 2013 Jan 8.

2.

A multilocus technique for risk evaluation of patients with neuroblastoma.

Ambros IM, Brunner B, Aigner G, Bedwell C, Beiske K, Bénard J, Bown N, Combaret V, Couturier J, Defferrari R, Gross N, Jeison M, Lunec J, Marques B, Martinsson T, Mazzocco K, Noguera R, Schleiermacher G, Speleman F, Stallings R, Tonini GP, Tweddle DA, Valent A, Vicha A, Roy NV, Villamon E, Ziegler A, Preuner S, Drobics M, Ladenstein R, Amann G, Schuit RJ, Pötschger U, Ambros PF.

Clin Cancer Res. 2011 Feb 15;17(4):792-804. doi: 10.1158/1078-0432.CCR-10-0830.

3.

Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA).

Lee ST, Kim HJ, Kim DK, Schuit RJ, Kim SH.

J Thromb Haemost. 2008 Apr;6(4):701-3. doi: 10.1111/j.1538-7836.2008.02905.x. Epub 2008 Jan 15. No abstract available.

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