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Plos One|July 27, 2010
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general populationPauline Chaste, Nathalie Clement, Oriane Mercati, et al.Nature Genetics|December 19, 2006
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersChristelle M Durand, Catalina Betancur, Tobias M Boeckers, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 26, 2008
Analysis of X chromosome inactivation in autism spectrum disordersXiaohong Gong, Elena Bacchelli, Francesca Blasi, et al.Journal of Pineal Research|May 28, 2011
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disordersPauline Chaste, Nathalie Clement, Hany Goubran Botros, et al.Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.Plos Genetics|September 5, 2014
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsClaire S Leblond, Caroline Nava, Anne Polge, et al.Pageof 6