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Showing articles 0 to 6 of 6 Filter Applied: screening (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 GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Somatic Mutations in Cerebral Cortical Malformations NEJM 371:733-743, Jamuar, S.S.,et al, 2014 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