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Haematologica|October 8, 2008
Prediction of molecular subtypes in acute myeloid leukemia based on gene expression profilingRoel G W Verhaak, Bas J Wouters, Claudia A J Erpelinck, et al.
Journal of Medical Genetics|April 23, 2017
Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutationIris H I M Hollink, Ans M W van den Ouweland, H Berna Beverloo, et al.
Blood|February 15, 2008
High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimatedSanne Lugthart, Ellen van Drunen, Yvette van Norden, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Clinical and cytogenetic analyses in uveal melanomaEmine Kilic, Walter van Gils, Elisabeth Lodder, et al.
Blood|May 21, 2011
Risk stratification of intermediate-risk acute myeloid leukemia: integrative analysis of a multitude of gene mutation and gene expression markersVeronika Rockova, Saman Abbas, Bas J Wouters, et al.
Blood|February 19, 2005
Asparagine synthetase expression is linked with L-asparaginase resistance in TEL-AML1-negative but not TEL-AML1-positive pediatric acute lymphoblastic leukemiaWendy A G Stams, Monique L den Boer, Amy Holleman, et al.
Genes, Chromosomes & Cancer|August 31, 2002
LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemiaAnne R M von Bergh, H Berna Beverloo, Paul Rombout, et al.
Genes, Chromosomes & Cancer|April 29, 2006
High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9Anne R M von Bergh, Ellen van Drunen, Elisabeth R van Wering, et al.
Blood|November 16, 2002
Sensitivity to L-asparaginase is not associated with expression levels of asparagine synthetase in t(12;21)+ pediatric ALLWendy A G Stams, Monique L den Boer, H Berna Beverloo, et al.
European Journal of Human Genetics : EJHG|March 8, 2012
A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation familyJeroen Knijnenburg, Yolande van Bever, Lorette O M Hulsman, et al.
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