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Journal Article
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
Pediatrics, ISSN 0031-4005, 11/2014, Volume 134, Issue 5, pp. 995 - 1005
Fragile X syndrome (FXS) is the most common known genetic cause of inherited intellectual disability and the most common known single-gene cause of autism... 
Sleep | Strabismus | Growth | Otitis media | Fragile X syndrome | Review | Gastrointestinal | Seizures | PARENT SURVEY | MENTAL-RETARDATION | otitis media | fragile X syndrome | STATUS EPILEPTICUS | MITRAL-VALVE-PROLAPSE | gastrointestinal | sleep | INTELLECTUAL DISABILITY | RECURRENT OTITIS-MEDIA | PRESCHOOL-AGE CHILDREN | strabismus | review | MARTIN-BELL SYNDROME | seizures | TYPICAL DEVELOPMENT | PEDIATRICS | growth | SLEEP PROBLEMS | Child Development Disorders, Pervasive - epidemiology | Gastrointestinal Diseases - epidemiology | Gastrointestinal Diseases - psychology | Humans | Seizures - diagnosis | Gastrointestinal Diseases - diagnosis | Nervous System Malformations - epidemiology | Heart Diseases - diagnosis | Heart Diseases - psychology | Child Development Disorders, Pervasive - psychology | Heart Diseases - epidemiology | Fragile X Syndrome - psychology | Seizures - epidemiology | Child Development Disorders, Pervasive - diagnosis | Nervous System Malformations - diagnosis | Quality of Life - psychology | Nervous System Malformations - psychology | Fragile X Syndrome - diagnosis | Fragile X Syndrome - epidemiology | Seizures - psychology | Complications and side effects | Care and treatment | Gastrointestinal diseases | Diagnosis | Risk factors | Autism | Pediatrics | Genetic disorders | Data collection | Systematic review | Sampling | Children & youth
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2001, Volume 3, Issue 5, pp. 359 - 371
The fragile X syndrome, an X-linked dominant disorder with reduced penetrance, is one of the most common forms of inherited mental retardation. The cognitive,... 
Fragile X syndrome | Review | Epidemiology | Mental retardation | FMR1 | FRAXA | RAPID ANTIBODY-TEST | HAIR ROOT ANALYSIS | fragile X syndrome | LEARNING-DIFFICULTIES | RETARDED MALES | RNA-BINDING PROTEIN | mental retardation | epidemiology | FULL MUTATION | review | DNA DIAGNOSIS | GENETICS & HEREDITY | CGG-REPEAT | MENTAL-RETARDATION PROTEIN | PRENATAL-DIAGNOSIS
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 4/2009, Volume 39, Issue 4, pp. 572 - 588
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 08/2008, Volume 45, Issue 8, pp. 498 - 499
Journal Article
Journal of Clinical Psychiatry, ISSN 0160-6689, 02/2011, Volume 72, Issue 2, pp. 175 - 182
Objective: The authors studied the lifetime prevalence of DSM-IV-TR psychiatric disorders in a population of adults with the fragile X premutation. Method: The... 
UNITED-STATES | GENERAL-POPULATION | STRUCTURED CLINICAL INTERVIEW | PSYCHIATRY | TREMOR/ATAXIA SYNDROME FXTAS | PSYCHIATRIC-DISORDER | NATIONAL-COMORBIDITY-SURVEY | FMR1 MESSENGER-RNA | SURVEY REPLICATION | PSYCHOLOGY, CLINICAL | AGE-OF-ONSET | PARKINSONS-DISEASE | Phobic Disorders - epidemiology | Mood Disorders - genetics | Humans | Middle Aged | Stress Disorders, Post-Traumatic - epidemiology | Anxiety Disorders - diagnosis | Male | Depressive Disorder, Major - epidemiology | Mood Disorders - epidemiology | DNA Mutational Analysis | Stress Disorders, Post-Traumatic - diagnosis | Phobic Disorders - diagnosis | Female | Phobic Disorders - genetics | Fragile X Syndrome - epidemiology | Fragile X Syndrome - genetics | Diagnostic and Statistical Manual of Mental Disorders | Genetic Predisposition to Disease - genetics | Cross-Sectional Studies | Comorbidity | RNA, Messenger - genetics | Anxiety Disorders - epidemiology | Phenotype | Depressive Disorder, Major - genetics | Panic Disorder - diagnosis | Mood Disorders - diagnosis | Panic Disorder - epidemiology | Anxiety Disorders - genetics | Aged | Fragile X Mental Retardation Protein - genetics | Depressive Disorder, Major - diagnosis | Stress Disorders, Post-Traumatic - genetics | Genetic Carrier Screening | Fragile X Syndrome - diagnosis | Panic Disorder - genetics | Depressive Disorders | Panic Disorder | Phobia | Anxiety Disorders | Americans | Adults | Genetic Markers | Neurological Symptoms | Epidemiology | PTSD (DSM-IV) | Mood Disorders | mood disorders | fragile X-associated tremor | FXTAS | anxiety disorders | Fragile X syndrome | ataxia syndrome | FMR1 gene
Journal Article
JAMA Neurology, ISSN 2168-6149, 03/2014, Volume 71, Issue 3, pp. 355 - 359
Fragile X syndrome (FXS), caused by a trinucleotide expansion (>200 CGG repeats) in the fragile X mental retardation gene (FMR1), is currently not included in... 
PREMUTATION | PREVALENCE | FMR1 | CLINICAL NEUROLOGY | Fragile X Syndrome - genetics | Neonatal Screening - standards | Genetic Testing - standards | Humans | Infant, Newborn | Fragile X Syndrome - diagnosis | Fragile X Syndrome - epidemiology
Journal Article
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2018, Volume 20, Issue 5, pp. 513 - 523
Journal Article
Journal Article