Ellen van Binsbergen

Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss.

Katherine Mathews, Karin Panzer, Matthew Deardorff, 2015, American journal of human genetics.

Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants

Edwin Cuppen, Wigard P. Kloosterman, Markus J. van Roosmalen, 2019, Genome Medicine.

Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants

Edwin Cuppen, Wigard P. Kloosterman, Markus J. van Roosmalen, 2019, Genome Medicine.