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Showing articles 0 to 8 of 8 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 Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy JAMA 325:467-475, Moreno-De-Luca, A.,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 Clinicopathological Conference, Chronic Candida Albicans Meningitis NEJM 387:641-650, Case 25-2022, 2022 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 SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016 Showing articles 0 to 8 of 8