A. V. D. Kevie-Kersemaekers

Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies

R. Pfundt, A. Green, W. Reardon, 2011, European Journal of Human Genetics.

Genome and Exome-Wide Studies Reveal Potential Predictive Efficacy Markers for Venetoclax and Rituximab (VenR) in Relapsed/Refractory Chronic Lymphocytic Leukemia (R/R CLL): Subgroup Analyses of the Murano Trial

T. Kipps, A. Langerak, A. Kater, 2019, Blood.

Estimates of live birth prevalence of children with Down syndrome in the period 1991–2015 in the Netherlands

R. Hochstenbach, A. Kooper, L. Zutven, 2017, Journal of intellectual disability research : JIDR.

Line Generation and characterization of a human iPSC line SANi 005-A containing the gray platelet associated heterozygous mutation p . Q 287 * in GFI 1 B

B. V. D. Reijden, C. Mellink, M. Lindern, 2017 .