Intellectual DisabilityEpilepsyMentally Disabled PersonsEpilepsy, GeneralizedDisability EvaluationIntellectual PropertyEpilepsy, Temporal LobeDisabled PersonsDevelopmental DisabilitiesMental Retardation, X-LinkedIntelligenceFaciesResidential FacilitiesIntelligence TestsAnticonvulsantsHaploinsufficiencyGenes, X-LinkedEpilepsies, MyoclonicAutistic DisorderLearning DisordersDown SyndromeFragile X SyndromeEpilepsy, ReflexChild Development Disorders, PervasiveSeizuresAdaptor Protein Complex 4Myoclonic Epilepsy, JuvenileEpilepsy, Tonic-ClonicInsurance, DisabilityAbnormalities, MultipleEducation of Intellectually DisabledMental DisordersFragile X Mental Retardation ProteinEpilepsy, Complex PartialElectroencephalographyDisabled ChildrenExomeSyndromeCommunication DisordersEpilepsy, Frontal LobeInstitutionalizationCommunication Aids for DisabledChromosomes, Human, XActivities of Daily LivingComparative Genomic HybridizationMicrocephalySegmental Duplications, GenomicEducation, SpecialChromosome DuplicationSexualityPrenatal InjuriesEpilepsy, RolandicMilieu TherapyGenetic Diseases, X-LinkedWestern AustraliaConsanguinityDNA Copy Number VariationsHuman CharacteristicsPedigreeCognition DisordersMetabolism, Inborn ErrorsMuscle HypotoniaPlasma Membrane Neurotransmitter Transport ProteinsEpilepsy, Post-TraumaticMortality, PrematurePatents as TopicBrain Diseases, Metabolic, InbornQuestionnairesCaregiversSeverity of Illness IndexPhenotypeBrainGroup HomesWechsler ScalesMotor Skills DisordersSpasms, InfantileGenes, RecessiveSmith-Magenis SyndromeSyriaLanguage Development DisordersMutationDe Lange SyndromeChild Behavior DisordersWilliams SyndromePensionsCraniofacial AbnormalitiesSelf-Injurious BehaviorClopenthixolIsraelMicrognathismNeuropsychological TestsMagnetic Resonance ImagingSocial BehaviorBrain Injury, ChronicComorbidityChromosome DeletionHuman RightsFoot Deformities, CongenitalNervous System DiseasesSeizures, Febrile