Showing results (321-330 of 872) with videos related to

Sort By:
Pageof 88
Neurology. Genetics|April 29, 2016
Analysis of rare copy number variation in absence epilepsiesLaura Addis, Richard E Rosch, Antonio Valentin, et al.
Neurology. Genetics|April 29, 2016
Compound heterozygote mutations in SPG7 in a family with adult-onset primary lateral sclerosisYi Yang, Lei Zhang, David R Lynch, et al.
Neurology. Genetics|April 29, 2016
Exonic deletion of SLC9A9 in autism with epilepsyMeeta Cardon, Karen D Evankovich, J Lloyd Holder
Neurology. Genetics|April 29, 2016
Copy number variants in absence epilepsy: Further complications of the pictureChantal Depondt
Neurology. Genetics|April 29, 2016
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanomaRivka Inzelberg, Yardena Samuels, Esther Azizi, et al.
Neurology. Genetics|April 12, 2016
Mutation in PNKP presenting initially as axonal Charcot-Marie-Tooth diseaseJosé Luiz Pedroso, Clarissa R R Rocha, Lucia I Macedo-Souza, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Neurology. Genetics|April 12, 2016
Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencingRumiko Izumi, Tetsuya Niihori, Toshiaki Takahashi, et al.
Neurology. Genetics|April 12, 2016
Polyneuropathy in a young Belgian patient: A novel heterozygous mutation in the WNK1/HSN2 geneJeroen de Filette, Danielle Hasaerts, Sara Seneca, et al.
Neurology. Genetics|April 12, 2016
Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variantsKaren Nuytemans, Lizmarie Maldonado, Aleena Ali, et al.
Pageof 88