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:
Weaving, Linda S.
Christodoulou, John
Williamson, Sarah L.
Friend, Kathie L.
McKenzie, Olivia L.D.
Archer, Hayley
Evans, Julie
Clarke, Angus
Pelka, Greogry J.
Tam, Patrick P.L.
Watson, Catherine
Lahooti, Hooshang
llaway, Carolyn J.
Bennetts, Bruce
Leonard, Helen
Gécz, Jozef
Citation: S. Weaving, Linda et al., Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation, American journal of human genetics , 75(6), 2004, pp. 1079-1093
Authors:
Burdon, Kathryn P.
McKay, James D.
Sale, Michèle M.
Russell-Eggitt, Isabelle M.
Wirth, M. Gabriela
Elder, James E.
Nicoll, Alan
Clarke, Michael P.
FitzGerald, Liesel M.
Stankovich, James M.
Shaw, Marie A.
Sharma, Shiwani
Gajovic, Srecko
Gruss, Peter
Ross, Shelley
Thomas, Paul
Voss, Anne K.
Thomas, Tim
Gécz, Jozef
Craig, Jamie E.
Mackey, David A.
Citation: P. Burdon, Kathryn et al., Mutations in a Novel Gene, NHS, Cause the Pleiotropic Effects of Nance-Horan Syndrome, Including Severe Congenital Cataract, Dental Anomalies, and Mental Retardation, American journal of human genetics , 73(5), 2003, pp. 1120-1130
Authors:
Kalscheuer, Vera M.
Tao, Jiong
Donnelly, Andrew
Hollway, Georgina
Schwinger, Eberdhard
Kübart, Sabine
Menzel, Corinna
Hoeltzenbein, Maria
Tommerup, Niels
Eyre, Helen
Harbord, Michael
Haan, Eric
Sutherland, Grant R.
Ropers, Hans-Hilger
Gécz, Jozef
Citation: M. Kalscheuer, Vera et al., Disruption of the Serine/Threonine Kinase 9 Gene Causes Severe X-Linked Infantile Spasms and Mental Retardation, American journal of human genetics , 72(6), 2003, pp. 1401-1411