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Highly sensitive MRD tests for ALL based on the IKZF1 Δ3-6 microdeletion.
Published in:
2012
By:
- Venn NC;
- van der Velden VH;
- de Bie M;
- Waanders E;
- Giles JE;
- Law T;
- Kuiper RP;
- de Haas V;
- Mullighan CG;
- Haber M;
- Marshall GM;
- Md N;
- van Dongen JJ;
- Sutton R;
- Venn, N C;
- van der Velden, V H J;
- de Bie, M;
- Waanders, E;
- Giles, J E;
- Law, T
Publication type:
Letter
Response to Palmirotta et al.: The frequency of the PRKCSH GAG trinucleotide repeat in PCLD patients.
Published in:
Clinical Genetics, 2011, v. 79, n. 4, p. 399, doi. 10.1111/j.1399-0004.2010.01537.x
By:
- Waanders, E.;
- Janssen, M. J.;
- Drenth, J. P. H.
Publication type:
Article
Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63.
Published in:
Clinical Genetics, 2010, v. 78, n. 1, p. 47, doi. 10.1111/j.1399-0004.2009.01353.x
By:
- Waanders, E.;
- Venselaar, H.;
- te Morsche, R. H. M.;
- de Koning, D. B.;
- Kamath, P. S.;
- Torres, V. E.;
- Somlo, S.;
- Drenth, J. P. H.
Publication type:
Article
Childhood neuroendocrine tumours: a descriptive study revealing clues for genetic predisposition.
Published in:
2017
By:
- Diets, I J;
- Nagtegaal, I D;
- Loeffen, J;
- de Blaauw, I;
- Waanders, E;
- Hoogerbrugge, N;
- Jongmans, M C J
Publication type:
journal article
Highly sensitive MRD tests for ALL based on the IKZF1 Δ3-6 microdeletion.
Published in:
Leukemia (08876924), 2012, v. 26, n. 6, p. 1414, doi. 10.1038/leu.2011.348
By:
- Venn, N C;
- van der Velden, V H J;
- de Bie, M;
- Waanders, E;
- Giles, J E;
- Law, T;
- Kuiper, R P;
- de Haas, V;
- Mullighan, C G;
- Haber, M;
- Marshall, G M;
- MD, Norris;
- van Dongen, J J M;
- Sutton, R
Publication type:
Article
Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia.
Published in:
Leukemia (08876924), 2011, v. 25, n. 2, p. 254, doi. 10.1038/leu.2010.275
By:
- Waanders, E.;
- van der Velden, V. H. J.;
- van der Schoot, C. E.;
- van Leeuwen, F. N.;
- van Reijmersdal, S. V.;
- de Haas, V.;
- Veerman, A. J.;
- van Kessel, A. Geurts;
- Hoogerbrugge, P. M.;
- Kuiper, R. P.;
- van Dongen, J. J. M.
Publication type:
Article
TET2 mutations in childhood leukemia.
Published in:
2011
By:
- Langemeijer, S. M. C.;
- Jansen, J. H.;
- Hooijer, J.;
- van Hoogen, P.;
- Stevens-Linders, E.;
- Massop, M.;
- Waanders, E.;
- van Reijmersdal, S. V.;
- Stevens-Kroef, M. J. P. L.;
- Zwaan, C. M.;
- van den Heuvel-Eibrink, M. M.;
- Sonneveld, E.;
- Hoogerbrugge, P. M.;
- Geurts van Kessel, A.;
- Kuiper, R. P.;
- van Kessel, A Geurts
Publication type:
Letter
IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL.
Published in:
Leukemia (08876924), 2010, v. 24, n. 7, p. 1258, doi. 10.1038/leu.2010.87
By:
- Kuiper, R. P.;
- Waanders, E.;
- van der Velden, V. H. J.;
- van Reijmersdal, S. V.;
- Venkatachalam, R.;
- Scheijen, B.;
- Sonneveld, E.;
- van Dongen, J. J. M.;
- Veerman, A. J. P.;
- van Leeuwen, F. N.;
- Geurts van Kessel, A.;
- Hoogerbrugge, P. M.
Publication type:
Article
Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma.
Published in:
2021
By:
- van Engelen, N.;
- van Dijk, F.;
- Waanders, E.;
- Buijs, A.;
- Vermeulen, M. A.;
- Loeffen, J. L. C.;
- Kuiper, R. P.;
- Jongmans, M. C. J.
Publication type:
Case Study

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