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Plos One|November 10, 2010
Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Gene|August 12, 2008
Nuclear localization of a novel human syntaxin 1B isoformSandrine Pereira, Annick Massacrier, Patrice Roll, et al.
Brain : a Journal of Neurology|January 10, 2006
Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortexSarah Jamali, Fabrice Bartolomei, Andrée Robaglia-Schlupp, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
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