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Showing articles 0 to 10 of 10 Filter Applied: exome sequencing (Click to remove) Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022 Clinicopathological Conference, Chronic Candida Albicans Meningitis NEJM 387:641-650, Case 25-2022, 2022 Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021 Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019 A 13-year-old boy with Chronic Ataxia and Developmental Delay Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 Showing articles 0 to 10 of 10