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Revue Medicale Suisse|April 19, 2018
[Care for unaccompanied minor migrant adolescents at the Youth Health Consultation: Support, psychotherapy and resilience]Cédric Devillé, Nelle LambertPlos Biology|June 13, 2008
Birth and rapid subcellular adaptation of a hominoid-specific CDC14 proteinLia Rosso, Ana Claudia Marques, Manuela Weier, et al.Cell|May 8, 2012
Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturationCécile Charrier, Kaumudi Joshi, Jaeda Coutinho-Budd, et al.Cell|June 2, 2018
Human-Specific NOTCH2NL Genes Expand Cortical Neurogenesis through Delta/Notch RegulationIkuo K Suzuki, David Gacquer, Roxane Van Heurck, et al.Human Molecular Genetics|September 18, 2012
Kinetochore KMN network gene CASC5 mutated in primary microcephalyAnne Genin, Julie Desir, Nelle Lambert, et al.Plos One|March 30, 2011
Genes expressed in specific areas of the human fetal cerebral cortex display distinct patterns of evolutionNelle Lambert, Marie-Alexandra Lambot, Angéline Bilheu, et al.Autism Research : Official Journal of the International Society for Autism Research|June 10, 2014
A familial heterozygous null mutation of MET in autism spectrum disorderNelle Lambert, Vanessa Wermenbol, Bruno Pichon, et al.Journal of Human Genetics|May 3, 2018
Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected motherNelle Lambert, Corinne Dauve, Emmanuelle Ranza, et al.Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.Nature|August 18, 2006
An RNA gene expressed during cortical development evolved rapidly in humansKatherine S Pollard, Sofie R Salama, Nelle Lambert, et al.Pageof 2