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Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome.
Published in:
Human Genetics, 2013, v. 132, n. 8, p. 885, doi. 10.1007/s00439-013-1295-2
By:
- Czeschik, J.;
- Voigt, C.;
- Alanay, Y.;
- Albrecht, B.;
- Avci, S.;
- FitzPatrick, D.;
- Goudie, D.;
- Hehr, U.;
- Hoogeboom, A.;
- Kayserili, H.;
- Simsek-Kiper, P.;
- Klein-Hitpass, L.;
- Kuechler, A.;
- López-González, V.;
- Martin, M.;
- Rahmann, S.;
- Schweiger, B.;
- Splitt, M.;
- Wollnik, B.;
- Lüdecke, H.
Publication type:
Article
Exon-level expression analyses identify MYCN and NTRK1 as major determinants of alternative exon usage and robustly predict primary neuroblastoma outcome.
Published in:
British Journal of Cancer, 2012, v. 107, n. 8, p. 1409, doi. 10.1038/bjc.2012.391
By:
- Schramm, A.;
- Schowe, B.;
- Fielitz, K.;
- Heilmann, M.;
- Martin, M.;
- Marschall, T.;
- Köster, J.;
- Vandesompele, J.;
- Vermeulen, J.;
- de Preter, K.;
- Koster, J.;
- Versteeg, R.;
- Noguera, R.;
- Speleman, F.;
- Rahmann, S.;
- Eggert, A.;
- Morik, K.;
- Schulte, J. H.
Publication type:
Article
The shortest common supersequence problem in a microarray production setting.
Published in:
Bioinformatics, 2003, v. 19, p. 156, doi. 10.1093/bioinformatics/btg1073
By:
- S. Rahmann
Publication type:
Article