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Journal of Intellectual Disability Research, ISSN 0964-2633, 02/2011, Volume 55, Issue 2, pp. 109 - 120
Background  Self‐injurious and aggressive behaviours are reported as components of some behavioural phenotypes but there are few studies comparing across... 
behavioural phenotype | impulsivity | challenging behaviour | hyperactivity | autism spectrum disorder | affect | Behavioural phenotype | Impulsivity | Challenging behaviour | Hyperactivity | Affect | Autism spectrum disorder | POPULATION | MENTAL-RETARDATION | INTELLECTUAL DISABILITIES PREVALENCE | ADULTS | MALADAPTIVE BEHAVIOR | EDUCATION, SPECIAL | CHILDREN | SMITH-MAGENIS-SYNDROME | FRAGILE-X-SYNDROME | REHABILITATION | DE-LANGE-SYNDROME | PRADER-WILLI-SYNDROME | Intervention | At Risk Persons | Emotional Response | Self Destructive Behavior | Genetic Disorders | Incidence | Phenomenology | Comparative Analysis | Behavior Problems | Pervasive Developmental Disorders | Questionnaires | Genetics | Injuries | Prader-Willi Syndrome - epidemiology | Chromosome Disorders - epidemiology | Angelman Syndrome - psychology | Prevalence | Humans | Middle Aged | Child, Preschool | Male | Genetic Diseases, Inborn - epidemiology | De Lange Syndrome - epidemiology | Case-Control Studies | Smith-Magenis Syndrome - epidemiology | Chromosome Disorders - psychology | Young Adult | Prader-Willi Syndrome - psychology | Oculocerebrorenal Syndrome - psychology | Self-Injurious Behavior - epidemiology | Abnormalities, Multiple - epidemiology | Adult | Female | Child | Abnormalities, Multiple - genetics | Fragile X Syndrome - epidemiology | Behavioral Symptoms - psychology | Child Development Disorders, Pervasive - epidemiology | Aggression | Comorbidity | Self-Injurious Behavior - psychology | Angelman Syndrome - epidemiology | Behavioral Symptoms - epidemiology | Cri-du-Chat Syndrome - epidemiology | Abnormalities, Multiple - psychology | Genetic Diseases, Inborn - psychology | Syndrome | Behavioral Symptoms - genetics | Child Development Disorders, Pervasive - psychology | Smith-Magenis Syndrome - psychology | Fragile X Syndrome - psychology | Adolescent | Cri-du-Chat Syndrome - psychology | Intellectual Disability - psychology | De Lange Syndrome - psychology | Oculocerebrorenal Syndrome - epidemiology | Prader-Willi syndrome | Genetic research | Prevalence studies (Epidemiology) | Genotype & phenotype | Autism | Comparative analysis | Self destructive behavior | Risk factors | Aggressiveness
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 4/2009, Volume 39, Issue 4, pp. 572 - 588
Journal Article
Journal of Allergy and Clinical Immunology: In Practice, ISSN 2213-2198, 2017, Volume 5, Issue 5, pp. 1344 - 1350.e3
Background Smith-Magenis syndrome (SMS) is a complex neurobehavioral disorder associated with recurrent otitis. Most SMS cases result from heterozygous... 
Internal Medicine | Allergy and Immunology | Chromosome 17p11.2 deletion | Smith-Magenis syndrome | FLCN | TOM1L2 | TNFRSF13B | Autoantibody | B-cell tolerance | Immune deficiency | IGA | HUMANS | COMMON VARIABLE IMMUNODEFICIENCY | IMMUNOLOGY | TUMORS | B-CELLS | TRANSMEMBRANE ACTIVATOR | TACI | ALLERGY | DISEASE | MUTATIONS | MICROARRAYS | Pneumonia | Prevalence | Immunologic Deficiency Syndromes - epidemiology | Humans | Child, Preschool | Infant | Male | Mutation - genetics | Sinusitis | Smith-Magenis Syndrome - epidemiology | Young Adult | Smith-Magenis Syndrome - genetics | B-Lymphocytes - immunology | DEAD Box Protein 58 - genetics | Smith-Magenis Syndrome - immunology | Adolescent | Otitis | Adult | Female | Immunologic Memory | Child | Immunoglobulin Class Switching | Intellectual Disability | Cohort Studies | Disease | Laboratories | Intellectual disabilities | Gastroenteritis | Genes | Families & family life | Antibodies | Infections | Arthritis | Malignancy | Atopy | Immunological diseases | Immunology | Tumor necrosis factor-TNF | Chromosomes | Chromosome 17 | Immune system | Medical research | Antigens | Immunological memory | Memory cells | Immunoglobulins | Immunodeficiency | Autoantigens | Allergies | Asthma | Children & youth | Pathology | Hospitals | Lymphocytes B | Monoclonal antibodies | Mutation | Tumors | immune deficiency | chromosome 17p11.2 deletion | autoantibody | FLCN and TOM1L2
Journal Article
Journal of Intellectual Disability Research, ISSN 0964-2633, 10/2008, Volume 52, Issue 10, pp. 830 - 841
Background  Behaviour problems and a preference for adult contact are reported to be prominent in the phenotype of Smith–Magenis syndrome. In this study we... 
behavioural phenotype | aggression | self‐injurious behaviour | functional analysis | Smith‐Magenis syndrome | Behavioural phenotype | Self-injurious behaviour | Smith-Magenis syndrome | Functional analysis | Aggression | SLEEP | 17P11.2 | MELATONIN | self-injurious behaviour | CIRCADIAN DISORDER | SELF-INJURIOUS-BEHAVIOR | EDUCATION, SPECIAL | INTERSTITIAL DELETION | BETA-ADRENERGIC ANTAGONISTS | P11.2P11.2 | REHABILITATION | DE-LANGE-SYNDROME | YOUNG-CHILDREN | Behavior Patterns | Behavior Problems | Mental Retardation | Reinforcement | Genetics | Adults | Children | Self Destructive Behavior | Environmental Influences | Interpersonal Relationship | Child Behavior Disorders - psychology | Self-Injurious Behavior - psychology | Humans | Child, Preschool | Male | Developmental Disabilities - genetics | Social Environment | Aggression - psychology | Syndrome | Intellectual Disability - genetics | Developmental Disabilities - epidemiology | Self-Injurious Behavior - genetics | Child Behavior Disorders - epidemiology | Adolescent | Self-Injurious Behavior - epidemiology | Female | Intellectual Disability - psychology | Child Behavior Disorders - genetics | Child | Interpersonal Relations | United Kingdom - epidemiology | Observer Variation | Developmental Disabilities - psychology | Intellectual Disability - epidemiology | Genotype & phenotype | Learning disabilities | Behavior disorders | Clinical psychology | Psychobiology | Genes
Journal Article