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	Title	Author(s)	Issue Date
	GRIN2A-related disorders: genotype and functional consequence predict phenotype Journal:Brain	Strehlow, V Heyne, HO Vlaskamp, DRM Marwick, KFM Rudolf, G de Bellescize, J Biskup, S Brilstra, EH Brouwer, OF Callenbach, PMC Hentschel, J Hirsch, E Kind, PC Mignot, C Platzer, K Rump, P Skehel, PA Wyllie, DJA Hardingham, GE van Ravenswaaj-Aris, CMA Lesca, G Lemke, JR Arzimanoglou, A Augustijn, PB Van Bogaert, P Bourry, H Burfeind, P Chu, WY Chung, BHY Doummar, D Edery, P Fattai-Valevski, A Fradin, M Gerard, M de Geus, C Gunning, S Hasaerts, D Helbig, I Heibig, KL Jamra, R Lyver, MJ Wassink-Ruifer, JSK Koolen, DA Lederer, D Lunsing, RJ Mathot, M Maurey, H Manascu, S Mishel, A Mirzaa, G Mittler, D Muhie, H Malter, RS Nava, C O'Brien, M van Piruderen-Nagler, E van Riesen, A Rougeot, C Sariaville, D Schieving, JH Syrte, S Veenstra-Knol, HE Verbeek, N Ville, D Vos, YJ Vrielynck, P Wagner, S Weckhuysen, S Willemsen, MH	2019
	Panel-Based Exome Sequencing for Neuromuscular Disorders as a Diagnostic Service Journal:Journal of Neuromuscular Diseases	Westra, D Schouten, MI Stunnenberg, BC Kusters, B Saris, CGJ Erasmus, CE van Engelen, BG Bulk, S Verschuuren-Bemelmans, CC Gerkes, EH de Geus, C van der Zwaag, PA Chan, S Chung, B Barge-Schaapveld, DQCM Kriek, M Sznajer, Y van Spaendonck-Zwarts, K van der Kooi, AJ Krause, A Schonewolf-Greulich, B de Die-Smu8lders, C Sallevelt, SCEH Krapels, IPC Rasmussen, M Maystadt, I Kievit, AJA Witting, N Pennings, M Meijer, R Gillissen, C Kamsteeg, EJ Voermans, NC	2019

Showing results 1 to 2 of 2