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| Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism |
| Authors: Laumonnier, F.; Shoubridge, C.; Antar, C.; Nguyen, L. S.; Van Esch, H.; Kleefstra, T.; Briault, S.; Fryns, J. P.; Hamel, B.; Chelly, J.; Ropers, H.-H.; Ronce, N.; Blesson, S.; Moraine, C.; Gécz, J.; Raynaud, M. | | Date of Publication (YYYY-MM-DD): 2009-02-24 | | Title of Journal: Molecular Psychiatry | | Volume: 2009 | | Start Page: 1 | | End Page: 10 | | Document Type: Article | | ID: 473311.0 |
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| Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation |
| Authors: Kleefstra, T.; Yntema, H. G.; Oudakker, A. R.; Banning, M. J. G.; Kalscheuer, Vera M.; Chelly, J.; Moraine, C.; Ropers, Hans-Hilger; Fryns, J-P; Janssen, I. M. J.; Sistermans, E. A.; Nillesen, W. N.; de Vries, L. B. A.; Hamel, B. C. J.; van Bokhoven, H. | | Date of Publication (YYYY-MM-DD): 2004-01-18 | | Title of Journal: Journal of Medical Genetics | | Volume: 41 | | Issue / Number: 5 | | Start Page: 394 | | End Page: 399 | | Document Type: Article | | ID: 224423.0 |
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| Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardation |
| Authors: Bienvenu, T.; Poirier, K.; Van Esch, H.; Hamel, B.; Moraine, C.; Fryns, J. P.; Ropers, H. H.; Beldjord, C.; Yntema, H. G.; Chelly, J. | | Date of Publication (YYYY-MM-DD): 2003-05 | | Title of Journal: Journal of Medical Genetics | | Volume: 40 | | Issue / Number: 5 | | Start Page: 357 | | End Page: 359 | | Document Type: Article | | ID: 126739.0 |
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