Belinda Dumee

Mutation in the AP4M1 Gene Provides a Model for Neuroaxonal Injury in Cerebral Palsy

Annemieke J.M.H. Verkerk, Rachel Schot, Belinda Dumee et al. · The American Journal of Human Genetics · 2009 · 172 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Neurological Disorder +13

Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

Renske Oegema, Annelies de Klein, Annemieke J.M.H. Verkerk et al. · Molecular Syndromology · 2010 · 48 citations · Full text

Prognostic and predictive performance of R-ISS with SKY92 in older patients with multiple myeloma: the HOVON-87/NMSG-18 trial

Rowan Kuiper, Sonja Zweegman, Mark van Duin et al. · Blood Advances · 2020 · 33 citations · Full text

Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome

Joyce M.G. Florisson, Irene M.J. Mathijssen, Belinda Dumee et al. · American Journal of Medical Genetics Part A · 2013 · 20 citations

Analytical Validation of SKY92 for the Identification of High-Risk Multiple Myeloma

Erik H. van Beers, Daphne Huigh, Lizanne Bosman et al. · Journal of Molecular Diagnostics · 2020 · 19 citations · Full text

Hematological Malignancy, Oncology, Analytical Validation +12