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Entries: 1-4  
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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
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
Authors: Laumonnier, Frédéric; Bonnet-Brilhault, Frédérique; Gomot, Marie; Blanc, Romuald; David, Albert; Moizard, Marie-Pierre; Raynaud, Martine; Ronce, Nathalie; Lemonnier, Eric; Calvas, Patrick; Laudier, Béatrice; Chelly, Jamel; Fryns, Jean-Pierre; Ropers, Hans-Hilger; Hamel, Ben C. J.; Andres, Christian; Barthélémy, Catherine; Moraine, Claude; Briault, Sylvain
Date of Publication (YYYY-MM-DD): 2004-02-12
Title of Journal: American Journal of Human Genetics
Volume: 74
Issue / Number: 3
Start Page: 552
End Page: 557
Document Type: Article
ID: 224730.0
FACL4, encoding fatty acid-CoA ligase 4, is mutated in
nonspecific X-linked mental retardation
Authors: Meloni, Ilaria; Muscettola, Maddalena; Raynaud, Martine; Longo, Ilaria; Bruttini, Mirella; Moizard, Marie-Pierre; Gomot, Marie; Chelly, Jamel; des Portes, Vincent; Fryns, Jean-Pierre; Ropers, Hans Hilger; Magi, Barbara; Bellan, Cristina; Volpi, Nila; Yntema, Helger G.; Lewis, Sarah E.; Schaffer, Jean E.; Renieri, Alessandra
Date of Publication (YYYY-MM-DD): 2002-03
Title of Journal: Nature Genetics
Volume: 30
Issue / Number: 4
Start Page: 436
End Page: 440
Document Type: Article
ID: 24181.0
In-frame deletion in MECP2 causes mild nonspecific mental retardation
Authors: Yntema, Helger G.; Oudakker, Astrid R.; Kleefstra, Tjitske; Hamel, Ben C. J.; van Bokhoven, Hans; Chelly, Jamel; Kalscheuer, Vera M.; Fryns, Jean-Pierre; Raynaud, Martine; Moizard, Marie-Pierre; Moraine, Claude
Date of Publication (YYYY-MM-DD): 2002-01
Title of Journal: American Journal of Medical Genetics
Volume: 107
Issue / Number: 1
Start Page: 81
End Page: 83
Document Type: Article
ID: 24374.0
Entries: 1-4  
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