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International Journal of Molecular Sciences|June 2, 2021
Genetic Dominant Variants in <i>STUB1,</i> Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16Yasaman Pakdaman, Siren Berland, Helene J Bustad, et al.Annals of Clinical and Translational Neurology|May 12, 2017
Diagnostic and cost utility of whole exome sequencing in peripheral neuropathyMaie Walsh, Katrina M Bell, Belinda Chong, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 29, 2022
Clinical impact of whole-genome sequencing in patients with early-onset dementiaAamira J Huq, Bryony Thompson, Mark F Bennett, et al.Cerebral Circulation - Cognition and Behavior|June 6, 2024
The protocol for an observational Australian cohort study of CADASIL: The AusCADASIL studyDanit G Saks, Beata Bajorek, Vibeke S Catts, et al.Journal of the Neurological Sciences|December 14, 2020
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspectiveDhamidhu Eratne, Amy Schneider, Ella Lynch, et al.Plos Genetics|August 31, 2011
Genomic analysis of the necrotrophic fungal pathogens Sclerotinia sclerotiorum and Botrytis cinereaJoelle Amselem, Christina A Cuomo, Jan A L van Kan, et al.Pageof 3