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Journal of Autism and Developmental Disorders, ISSN 0162-3257, 4/2009, Volume 39, Issue 4, pp. 572 - 588
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
Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 8, pp. 794 - 809
Objective Current research suggests that the causes of autism spectrum disorders (ASD) are multifactorial and include both genetic and environmental factors.... 
Pediatrics | Psychiatry | autism spectrum disorders | epigenetics | genetics | GENOTYPE-PHENOTYPE CORRELATIONS | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | NEUROTROPHIC FACTOR BDNF | CHINESE HAN POPULATION | SEROTONIN TRANSPORTER GENE | PERVASIVE DEVELOPMENTAL DISORDERS | BECKWITH-WIEDEMANN-SYNDROME | FRAGILE-X-SYNDROME | PEDIATRICS | IN-VITRO FERTILIZATION | SYNDROME CRITICAL REGION | PRADER-WILLI-SYNDROME | Autism | Etiology | Pervasive Developmental Disorders | Mental Retardation | Evidence | Genetics | Environmental Influences | Cognitive Development | Symptoms (Individual Disorders) | Megalencephaly - psychology | Angelman Syndrome - psychology | Humans | Rett Syndrome - psychology | Angelman Syndrome - diagnosis | Social Environment | CHARGE Syndrome - psychology | Turner Syndrome - diagnosis | Prader-Willi Syndrome - psychology | Child Development Disorders, Pervasive - diagnosis | Angelman Syndrome - genetics | Prader-Willi Syndrome - genetics | Child | Fragile X Syndrome - genetics | Genetic Predisposition to Disease - psychology | Megalencephaly - genetics | Prader-Willi Syndrome - diagnosis | Genetic Predisposition to Disease - genetics | Genetic Association Studies | Rett Syndrome - diagnosis | Comorbidity | Risk Factors | CHARGE Syndrome - diagnosis | Chromosomes, Human, Pair 15 - genetics | Megalencephaly - diagnosis | Child Development Disorders, Pervasive - psychology | Child Development Disorders, Pervasive - genetics | Epigenesis, Genetic - genetics | Fragile X Syndrome - psychology | Adolescent | Turner Syndrome - genetics | CHARGE Syndrome - genetics | Rett Syndrome - genetics | Fragile X Syndrome - diagnosis | Psychological aspects | Epigenetic inheritance | Genetic aspects | Epigenetics | Child psychology | Gene expression | Genomics | Deoxyribonucleic acid--DNA
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 12/2017, Volume 217, Issue 6, pp. 691.e1 - 691.e6
Since its debut in 2011, cell-free fetal DNA screening has undergone rapid expansion with respect to both utilization and coverage. However, conclusive data... 
amniocentesis | trisomy 13 | trisomy 21 | 47,XXY | noninvasive prenatal testing | noninvasive prenatal screening | 47,XXX | 47,XYY | cell-free DNA | NIPT | prenatal diagnosis | microdeletion syndrome | trisomy 18 | CHROMOSOMAL MICROARRAY | TRISOMIES 21 | FREE DNA | RISK | CLINICAL-EXPERIENCE | OBSTETRICS & GYNECOLOGY | FETAL ANEUPLOIDIES | Chromosome Disorders - blood | Predictive Value of Tests | Turner Syndrome - blood | Cri-du-Chat Syndrome - diagnosis | Humans | Angelman Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - genetics | Turner Syndrome - diagnosis | Sex Chromosome Disorders of Sex Development - blood | Trisomy 18 Syndrome - diagnosis | Cri-du-Chat Syndrome - genetics | Klinefelter Syndrome - blood | Klinefelter Syndrome - genetics | Sex Chromosome Aberrations | Microarray Analysis | Karyotyping | Down Syndrome - blood | Angelman Syndrome - genetics | Chorionic Villi Sampling | Chromosome Disorders - diagnosis | Prader-Willi Syndrome - genetics | Female | Down Syndrome - diagnosis | Amniocentesis | Prader-Willi Syndrome - diagnosis | Trisomy 13 Syndrome - genetics | Chromosomes, Human, X - genetics | Prader-Willi Syndrome - blood | Prenatal Diagnosis | In Situ Hybridization, Fluorescence | Cri-du-Chat Syndrome - blood | Pregnancy | Trisomy 18 Syndrome - blood | Sex Chromosome Disorders of Sex Development - diagnosis | Trisomy - diagnosis | Trisomy - genetics | Trisomy 13 Syndrome - blood | Cell-Free Nucleic Acids - blood | Trisomy 18 Syndrome - genetics | Down Syndrome - genetics | Klinefelter Syndrome - diagnosis | Turner Syndrome - genetics | Angelman Syndrome - blood | Trisomy 13 Syndrome - diagnosis | Chromosome Disorders - genetics | DNA microarrays | Medical screening | Pregnant women | Chromosomes | Analysis
Journal Article
Journal of Intellectual Disability Research, ISSN 0964-2633, 10/2009, Volume 53, Issue 10, pp. 852 - 873
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1995, Volume 4, Issue 5, pp. 801 - 806
Journal Article
Journal Article