Martine van Belzen

Phenotype and genotype in 52 patients with Rubinstein–Taybi syndrome caused by <i>EP300</i> mutations

Patricia Fergelot, Martine van Belzen, Julien Van‐Gils et al. · American Journal of Medical Genetics Part A · 2016 · 122 citations

Association between the <i>CHRM2</i> gene and intelligence in a sample of 304 Dutch families

M.F. Gosso, Martine van Belzen, Eco J. C. de Geus et al. · Genes Brain & Behavior · 2006 · 47 citations · Full text

<i><scp>CREBBP</scp></i> and <i><scp>EP</scp>300</i> mutational spectrum and clinical presentations in a cohort of <scp>S</scp>wedish patients with <scp>R</scp>ubinstein–<scp>T</scp>aybi syndrome

Josephine Wincent, Aron Luthman, Martine van Belzen et al. · Molecular Genetics & Genomic Medicine · 2015 · 30 citations · Full text

Rubinstein–Taybi syndrome (CREBBP, EP300)

Martine van Belzen, Oliver Bartsch, Didier Lacombe et al. · European Journal of Human Genetics · 2010 · 29 citations · Full text

Rubinstein–taybi Syndrome, Mendelian Disorder, Genetic Disorder +3

TEAM: a tool for the integration of expression, and linkage and association maps

Lude Franke, Harm van Bakel, Begoña Diosdado et al. · European Journal of Human Genetics · 2004 · 28 citations · Full text

Engineering, Data Science, Data Mining +12