Next-generation phenotyping using computer vision algorithms in rare genomic neurodevelopmental disorders by Van Der Donk, R, Jansen, S, Schuurs-Hoeijmakers, J, Koolen, D, Goltstein, L, Hoischen, A, Brunner, H, Kemmeren, P, Nellaker, C, Vissers, L, De Vries, B, Hehir-Kwa, J

Clinical significance of de novo and inherited copy-number variation. by Vulto-van Silfhout, A, Hehir-Kwa, J, van Bon, B, Schuurs-Hoeijmakers, J, Meader, S, Hellebrekers, C, Thoonen, I, de Brouwer, A, Brunner, H, Webber, C, Pfundt, R, de Leeuw, N, de Vries, B

Clinical Significance of De Novo and Inherited Copy-Number Variation by Vulto-van Silfhout, A, Hehir-Kwa, J, van Bon, B, Schuurs-Hoeijmakers, J, Meader, S, Hellebrekers, C, Thoonen, I, de Brouwer, A, Brunner, H, Webber, C, Pfundt, R, de Leeuw, N, De Vries, B