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The European Journal of Neuroscience|March 8, 2006
The role of ARX in cortical developmentGaëlle Friocourt, Karine Poirier, Sonja Rakić, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Loss of Function of KCNC1 is associated with intellectual disability without seizuresKarine Poirier, Géraldine Viot, Laura Lombardi, et al.
Canadian Journal on Aging = La Revue Canadienne Du Vieillissement|March 8, 2022
Experience and Appreciation of Health Care Teams Regarding a New Model of Pharmaceutical Care in Long-Term Care SettingsVéronique Turcotte, Edeltraut Kröger, Rachel Rouleau, et al.
Human Mutation|June 7, 2017
CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsyKarine Poirier, Laurence Hubert, Géraldine Viot, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
The ARX mutations: a frequent cause of X-linked mental retardationMagdalena Nawara, Krzysztof Szczaluba, Karine Poirier, et al.
Acta Neuropathologica|April 9, 2010
Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotypeMagalie Lecourtois, Karine Poirier, Gaëlle Friocourt, et al.
Psychiatric Genetics|April 2, 2019
Anorexia nervosa is associated with Neuronatin variantsLaura Lombardi, Corinne Blanchet, Karine Poirier, et al.
Gene|September 16, 2018
Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequencesNicolas Lebrun, Claire Mehler-Jacob, Karine Poirier, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
In vitro follicular growth affects oocyte imprinting establishment in miceAntoine Kerjean, Philippe Couvert, Thomas Heams, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|August 10, 2017
Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathyClaude Besmond, Dominique Valla, Laurence Hubert, et al.
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