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Cell|March 7, 1998
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling proteinJ G Gleeson, K M Allen, J W Fox, et al.The Review of Scientific Instruments|December 3, 2022
X-ray imaging and radiation transport effects on cylindrical implosionsG Pérez-Callejo, M Bailly-Grandvaux, R Florido, et al.The Review of Scientific Instruments|July 10, 2021
Diagnosing plasma magnetization in inertial confinement fusion implosions using secondary deuterium-tritium reactionsH Sio, J D Moody, D D Ho, et al.Neurology|October 21, 2009
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+A Poduri, Y Wang, D Gordon, et al.Neuron|January 1, 1996
Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical developmentY Z Ekşioğlu, I E Scheffer, P Cardenas, et al.Neurology|March 9, 2005
Reading impairment in the neuronal migration disorder of periventricular nodular heterotopiaB S Chang, J Ly, B Appignani, et al.Neurology|May 26, 2004
Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformationB S Chang, X Piao, C Giannini, et al.Annals of Neurology|February 9, 2000
Genetic and neuroradiological heterogeneity of double cortex syndromeJ G Gleeson, R F Luo, P E Grant, et al.Neurology|January 13, 2012
FLNA genomic rearrangements cause periventricular nodular heterotopiaK R Clapham, T W Yu, V S Ganesh, et al.Journal of Medical Genetics|July 22, 2005
The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationL Basel-Vanagaite, R Attia, M Yahav, et al.Pageof 24