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Entries: 1-4  
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium
Authors: de Brouwer, Arjan P.M.; Yntema, Helger G.; Kleefstra, Tjitske; Lugtenberg, Dorien; Oudakker, Astrid R.; de Vries, Bert B. A.; van Bokhoven, Hans; van Esch, Hilde; Frints, Suzanne G. M.; Froyen, Guy; Fryns, Jean-Pierre; Raynaud, Martine; Moizard, Marie-Pierre; Ronce, Nathalie; Bensalem, Anissa; Moraine, Claude; Poirier, Karine; Castelnau, Laetitia; Saillour, Yoann; Bienvenu, Thierry; Beldjord, Chérif; des Portes, Vincent; Chelly, Jamel; Turner, Gillian; Fullston, Tod; Gecz, Jozef; Kuss, Andreas W.; Tzschach, Andreas; Jensen, Lars Riff; Lenzner, Steffen; Kalscheuer, Vera M.; Ropers, Hans-Hilger; Hamel, Ben C.J.
Date of Publication (YYYY-MM-DD): 2007-01-12
Title of Journal: Human Mutation
Volume: 28
Issue / Number: 2
Start Page: 207
End Page: 208
Document Type: Article
ID: 333783.0
Full text / Content available
Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males
Authors: Poirier, Karine; Francis, Fiona; Hamel, Ben; Moraine, Claude; Fryns, Jean Pierre; Ropers, Hans-Hilger; Chelly, Jamel; Bienvenu, Thierry
Date of Publication (YYYY-MM-DD): 2005-03-16
Title of Journal: Druckausgaben (und Verfilmungen)
Volume: 13
Issue / Number: 5
Start Page: 523
End Page: 524
Document Type: Article
ID: 271565.0
Full text / Content available
ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.
Authors: Bienvenu, Thierry; Poirier, Karine; Friocourt, Gaelle; Bahi, Nadia; Beaumont, Delphine; Fauchereau, Fabien; Jeema, Lamia Ben; Zemni, Ramzi; Vinet, Marie-Claude; Francis, Fiona; Couvert, Philippe; Gomot, Marie; Moraine, Claude; Bokhoven, Hans van; Kalscheuer, Vera; Frints, Suzanne; Gecz, Josef; Ohzaki, Kanae; Chaabouni, Habiba; Fryns, Jean-Pierre; Desportes, Vincent; Beldjord, Cherif; Chelly, Jamel
Date of Publication (YYYY-MM-DD): 2002-04
Title of Journal: Human Molecular Genetics
Volume: 11
Issue / Number: 8
Start Page: 981
End Page: 991
Document Type: Article
ID: 24040.0
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation
Authors: Zanni, Ginevra; van Esch, Hilde; Bensalem, Anissa; Saillour, Yoann; Poirier, Karine; Castelnau, Laetitia; Ropers, Hans-Hilger; . de Brouwer, Arjan P. M.; Laumonnier, Fréderic; Fryns, Jean-Pierre; Chelly, Jamel
Title of Journal: Neurogenetics
Volume: 11
Issue / Number: 2
Start Page: 251
End Page: 255
Document Type: Article
ID: 536143.0
Entries: 1-4  
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