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The Journal of Physical Chemistry. A|September 6, 2024
Multireference Averaged Quadratic Coupled Cluster (MR-AQCC) Study of the Geometries and Energies for ortho-, meta- and para-BenzyneKhanh Vu, Joshua Pandian, Boyi Zhang, et al.American Journal of Medical Genetics. Part A|May 16, 2012
Asymmetric polymicrogyria and periventricular nodular heterotopia due to mutation in ARXRenske Oegema, Anneke Maat-Kievit, Maarten H Lequin, et al.Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, 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.Brain : a Journal of Neurology|August 12, 2020
Definitions and classification of malformations of cortical development: practical guidelinesMariasavina Severino, Ana Filipa Geraldo, Norbert Utz, et al.Plos Genetics|April 27, 2018
Altered distribution of ATG9A and accumulation of axonal aggregates in neurons from a mouse model of AP-4 deficiency syndromeRaffaella De Pace, Miguel Skirzewski, Markus Damme, et al.Human Molecular Genetics|May 15, 2010
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulinsRavinesh A Kumar, Daniela T Pilz, Timothy D Babatz, et al.American Journal of Medical Genetics. Part A|February 4, 2005
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch familiesG M S Mancini, C E Catsman-Berrevoets, I F M de Coo, et al.Journal of Applied Microbiology|December 16, 2020
Detection of environmental contamination with feline and canine parvoviruses: new perspectives and challengesM L Marenzoni, M B Conti, E Rossi, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 12, 2019
EML1-associated brain overgrowth syndrome with ribbon-like heterotopiaRenske Oegema, George McGillivray, Richard Leventer, et al.Pageof 44