Browse Items (2 total)
Sort by:
This site uses Google Analytics to track site traffic and other metrics. If you would like to allow the use of Google Analytics please click Opt In below. This will associate a cookie with your browser.
Tags: 0 (Methyl-CpG-Binding Protein 2), 2016, Adolescent, Adult, American Journal of Medical Genetics Part A, Anderson B, Boban S, characteristics, Child, Child Preschool, Downs J, Epilepsy/di [diagnosis], Epilepsy/ge [Genetics], Epstein A, Genetic Association Studies, Genotype, Humans, Infant, Infant Newborn, Leonard H, Methyl-CpG-Binding Protein 2/ge [Genetics], Middle Aged, Murphy N, Mutation, Phenotype, Rett syndrome, Rett Syndrome/di [Diagnosis], Rett Syndrome/ge [Genetics], Rett Syndrome/pp [Physiopathology], Severity Of Illness Index, sleep disturbance/disorders, Sleep Wake Disorders/di [Diagnosis], Sleep Wake Disorders/ge [Genetics], Trajectory, Wong K, Young Adult
Tags: 2009, Backlog, Brain Diseases, Electroencephalography, Epilepsy/cn [Congenital], Epilepsy/ge [Genetics], Epilepsy/th [Therapy], Humans, Inborn/ge [Genetics], Inborn/th [Therapy], Infant, Journal Article, Journal Of Inherited Metabolic Disease, KT Synthesis, Metabolic, Newborn, Pearl PL, Pyridoxine/ph [Physiology], Seizures/cn [Congenital], Seizures/et [Etiology], Seizures/th [Therapy], Vitamin B 6 Deficiency/ge [Genetics], Vitamin B 6 Deficiency/pp [Physiopathology]