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:
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
Authors:
Kolehmainen, Juha
Black, Graeme C.M.
Saarinen, Anne
Chandler, Kate
Clayton-Smith, Jill
Träskelin, Ann-Liz
Perveen, Rahat
Kivitie-Kallio, Satu
Norio, Reijo
Warburg, Mette
Fryns, Jean-Pierre
de la Chapelle, Albert
Lehesjoki, Anna-Elina
Citation: Kolehmainen, Juha et al., Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport, American journal of human genetics , 72(6), 2003, pp. 1359-1369
Authors:
Irrthum, Alexandre
Devriendt, Koenraad
Chitayart, David
Matthijis, Gert
Glade, Conrad
Steijlen, Peter M.
Fryns, Jean-Pierre
Steensel, Maurice A., Van
Vikkula, Miikka
Citation: Irrthum, Alexandre et al., Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia, American journal of human genetics , 72(6), 2003, pp. 1470-1478