Authors: Riff Jensen, Lars Amende, Marion Gurok, Ulf Moser, Betina Gimmel, Verena Tzschach, Andreas Janecke, Andreas R. Tariverdian, Gholamali Chelly, Verena Fryns, Jean-Pierre Van Esch, Hilde Kleefstra, Tjitske Hamel, Ben Moraine, Claude Gécz, Jozef Turner, Gillian Reinhardt, Richard Kalscheuer, Vera M. Ropers, Hans-Hilger Lenzner, Steffen

Citation: Riff Jensen, Lars et al., Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation, American journal of human genetics , 76(2), 2005, pp. 227-236

Authors: Lugtenberg, Dorien Yntema, Helger G. Banning, Martijn J.G. Oudakker, Astrid R. Firth, Helen V. Willatt, Lionel Raynaud, Martine Kleefstra, Tjitske Fryns, Jean-Pierre Ropers, Hans-Hilger Chelly, Jamel Moraine, Claude Gécz, Jozef Van Reeuwijk, Jeroen Nabuurs, Sander B. De Vries, Bert B.A. Hamel,Ben C. J. De Brouwer, Arjan P.M. Van Bokhoven, Hans

Citation: Lugtenberg, Dorien et al., ZNF674: A New Krüppel-Associated Box.Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation, American journal of human genetics , 78(2), 2006, pp. 265-278

Authors: Van Esch, Hilde Bauters, Marijke Ignatius, Jaakko Jansen, Mieke Raynaud, Martine Hollanders, Karen Lugtenberg, Dorien Bienvenu, Thierry Riff Jensen, Lars Gécz, Jozef Moraine, Claude Marynen, Peter Fryns, Jean-Pierre Froyen, Guy

Citation: Van Esch, Hilde et al., Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males, American journal of human genetics , 77(3), 2005, pp. 442-453

Authors: Stoppa-Lyonnet, Dominique Duponchel, Christiane Meo, Tommaso Laurent, Jérôme Carter, Philip E. Arala-Chaves, Mario Cohen, Jacques H. M. Dewald, Georg Goetz, Joelle Hauptmann, Georges Lagrue, Gilbert Lesavre, Philippe Lopez-Trascasa, Margarita Misiano, Gabriella Moraine, Claude Sobel, Alain Späth, Pierre J. Tosi, Mario

Citation: Stoppa-lyonnet, Dominique et al., Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients, American journal of human genetics , 49-II(5), 1991, pp. 1055-1062

Authors: Shoichet, Sarah A. Hoffmann, Kristen Menzel, Corinna Trautmann, Udo Moser, Bettina Hoeltzeinbein, Maria Echenne, Bernard Partington, Michael Bokhoven, Hans, Van Moraine, Claude Fryns, Jean-Pierre Chelly, Jamel Rott, Hans-Dieter Ropers, Hans-Hilger Kalscheuer, Vera M.

Citation: A. Shoichet, Sarah et al., Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation, American journal of human genetics , 73(6), 2003, pp. 1341-1354