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Springer Nature4
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Human Genetics2
Journal of Molecular Medicine1
NeuroMolecular Medicine1
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Jamel Chelly results 4 · Newest (Page 1/1, per page 25)
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Astrocyte Transcriptome from the Mecp2308-Truncated Mouse Model of Rett SyndromeNARA Subscribed
NeuroMolecular Medicine · 2015 · Vol. 17 · Issue 4 · Springer
Chloé Delépine; Juliette Nectoux; Franck Letourneur; Véronique Baud; Jamel Chelly; Pierre Billuart; Thierry Bienvenu
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Cell cloning-based transcriptome analysis in cyclin-dependent kinase-like 5 mutation patients with severe epileptic encephalopathyNARA Subscribed
Journal of Molecular Medicine · 2011 · Vol. 89 · Issue 2 · Springer
Juliette Nectoux; Yann Fichou; Nicolas Cagnard; Nadia Bahi-Buisson; Patrick Nusbaum; Franck Letourneur; Jamel Chelly; Thierry Bienvenu
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Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic regionNARA Subscribed
Human Genetics · 2007 · Vol. 121 · Issue 5 · Springer
Guy Froyen; Marijke Bauters; Jackie Boyle; Hilde Van Esch; Karen Govaerts; Hans van Bokhoven; Hans-Hilger Ropers; Claude Moraine; Jamel Chelly; Jean-Pierre Fryns; Peter Marynen; Jozef Gecz; Gillian Turner
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Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardationNARA Subscribed
Human Genetics · 2006 · Vol. 118 · Issue 5 · Springer
Olivier Hagens; Aline Dubos; Fatima Abidi; Gotthold Barbi; Laura Van Zutven; Maria Hoeltzenbein; Niels Tommerup; Claude Moraine; Jean-Pierre Fryns; Jamel Chelly; Hans van Bokhoven; Jozef Gécz; Hélène Dollfus; Hans-Hilger Ropers; Charles E. Schwartz; Rita de Cassia Stocco dos Santos; Vera Kalscheuer; André Hanauer
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