Childhood neuroendocrine tumours: a descriptive study revealing clues for genetic predisposition

por Diets, I J, Nagtegaal, I D, Loeffen, J, de Blaauw, I, Waanders, E, Hoogerbrugge, N, Jongmans, M C J
Publicado 2017

Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma

por van Engelen, N., van Dijk, F., Waanders, E., Buijs, A., Vermeulen, M. A., Loeffen, J. L. C., Kuiper, R. P., Jongmans, M. C. J.
Publicado 2021

A novel germline PAX5 single exon deletion in a pediatric patient with precursor B-cell leukemia

por van Engelen, N., Roest, M., van Dijk, F., Sonneveld, E., Bladergroen, R., van Reijmersdal, S. V., van der Velden, V. H. J., Hoogeveen, P. G., Kors, W. A., Waanders, E., Jongmans, M. C. J., Kuiper, R. P.
Publicado 2023

Highly sensitive MRD tests for ALL based on the IKZF1 Δ3–6 microdeletion

por 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
Publicado 2012