| Authors: |
Cheung JS; Department of Pediatrics, Erasmus MC, Rotterdam, 3000 CB, the Netherlands., van Woerden GM; Department of Neuroscience, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Department of Clinical Genetics, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, the Netherlands. Electronic address: g.vanwoerden@erasmusmc.nl., Veenma DCM; Department of Pediatrics, Erasmus MC, Rotterdam, 3000 CB, the Netherlands; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, Rotterdam, 3015 GD, the Netherlands; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, the Netherlands. |
