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Showing articles 0 to 8 of 8 Filter Applied: exome sequencing (Click to remove) 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 A 26-Year-OldWoman with Headache and Eosinophilia Neurol 104:e213434, Goh,W.G.W.,et al, 2025 A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025 A 51-Year-Old Woman with Abnormal Corups Callosum Signal JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024 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 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 8 of 8