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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
	Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprungs disease Journal:Human Molecular Genetics	Amiel, J Attie, T Jan, D Pelet, A Edery, P Bidaud, C Lacombe, D Tam, PKH Simeoni, J Flori, E Nihoul-Fekete, C Munnich, A Lyonnet, S	1996

Showing results 1 to 2 of 2