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Showing articles 0 to 6 of 6 Filter Applied: exome sequencing (Click to remove) 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 Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022 Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021 A 13-Year-Old Boy with Subacute-Onset Spastic Gait JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021 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 Showing articles 0 to 6 of 6