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Seminars in Cell & Developmental Biology|August 1, 2022
Tubulin mutations in human neurodevelopmental disordersCamille Maillard, Charles Joris Roux, Fabienne Charbit-Henrion, et al.
European Journal of Medical Genetics|May 15, 2018
TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephalyMara Cavallin, Camille Maillard, Marie Hully, et al.
European Journal of Medical Genetics|August 20, 2018
Recurrent RTTN mutation leading to severe microcephaly, polymicrogyria and growth restrictionMara Cavallin, Amandine Bery, Camille Maillard, et al.
European Journal of Medical Genetics|October 1, 2018
Mutations in TBR1 gene leads to cortical malformations and intellectual disabilityNancy Vegas, Mara Cavallin, Tjitske Kleefstra, et al.
European Journal of Medical Genetics|July 20, 2021
Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndromeNina-Maria Wilpert, Florent Marguet, Camille Maillard, et al.
American Journal of Medical Genetics. Part A|February 8, 2017
Prenatal and postnatal presentations of corpus callosum agenesis with polymicrogyria caused by EGP5 mutationCamille Maillard, Mara Cavallin, Kevin Piquand, et al.
Journal of Neuropathology and Experimental Neurology|April 11, 2017
Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 MutationsAnnie Laquerriere, Camille Maillard, Mara Cavallin, et al.
Cell Reports|August 8, 2019
Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary CiliaAna Uzquiano, Carmen Cifuentes-Diaz, Ammar Jabali, et al.
Journal of Visualized Experiments : Jove|April 7, 2022
2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical DevelopmentLucile Boutaud, Marie Michael, Céline Banal, et al.
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