Joris A. Veltman

Genomic microarrays in mental retardation: A practical workflow for diagnostic applications

Erik Sistermans, Nicole de Leeuw, Rolph Pfundt, 2009, Human mutation.

A Post‐Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

Christian Gilissen, Ilse Feenstra, Nienke Wieskamp, 2013, Human mutation.

Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: A multicenter study

Luminita Moruz, Andreas Dufke, Olaf Riess, 2009, Human mutation.

Detection of Clinically Relevant Copy Number Variants with Whole‐Exome Sequencing

Todd Richmond, Rolph Pfundt, L. Vissers, 2013, Human mutation.