Margreet Walinga

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

S. Scherer, A. C. Lionel, C. Marshall, 2016, Genetics in Medicine.

Detection of Childhood Visual Impairment in At-Risk Groups

N. Schalij-Delfos, H. Evenhuis, M. Genderen, 2007 .

Consensus recommendations on altered sensory functioning in Phelan-McDermid syndrome.

S. Jesse, G. Van Buggenhout, Margreet Walinga, 2023, European journal of medical genetics.

Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey

A. Landlust, Margreet Walinga, Sylvia A. Koza, 2023, European Journal of Medical Genetics.