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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 | Index Medicus
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 | Index Medicus | Abridged Index Medicus
Journal Article
Journal Article
Current Psychiatry Reviews, ISSN 1573-4005, 2014, Volume 10, Issue 2, pp. 168 - 181
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 8/2011, Volume 41, Issue 8, pp. 1019 - 1032
Journal Article
Experimental and Clinical Endocrinology & Diabetes, ISSN 0947-7349, 11/2012, Volume 120, Issue 10, pp. 579 - 585
Abstract Background: Several genetic syndromes are associated with diabetes mellitus (DM). This study aimed to analyse data from the DPV database with regard... 
Article | Klinefelter syndrome | Friedreich ataxia | Pediatric diabetology | Prader-Willi syndrome | Turner syndrome | Alström syndrome | YOUNG-ADULTS | DOWNS-SYNDROME | INCREASED PREVALENCE | TURNER-SYNDROME | ALSTROM-SYNDROME | KLINEFELTERS-SYNDROME | GHRELIN LEVELS | ENDOCRINOLOGY & METABOLISM | BODY-MASS INDEX | Alstrom syndrome | PRADER-WILLI-SYNDROME | Diabetes Mellitus, Type 1 - epidemiology | Glycated Hemoglobin A - analysis | Prader-Willi Syndrome - epidemiology | Genetic Diseases, Inborn - blood | Prevalence | Prospective Studies | Turner Syndrome - blood | Diabetic Nephropathies - etiology | Humans | Male | Down Syndrome - physiopathology | Diabetes Mellitus, Type 1 - complications | Genetic Diseases, Inborn - epidemiology | Diabetes Mellitus, Type 2 - epidemiology | Turner Syndrome - epidemiology | Diabetes Mellitus, Type 1 - etiology | Diabetes Mellitus, Type 2 - immunology | Prader-Willi Syndrome - physiopathology | Turner Syndrome - physiopathology | Down Syndrome - blood | Autoantibodies - analysis | Diabetes Mellitus, Type 2 - etiology | Female | Prader-Willi Syndrome - immunology | Diabetes Mellitus, Type 1 - immunology | Diabetic Retinopathy - etiology | Child | Dyslipidemias - etiology | Diabetes Mellitus, Type 2 - complications | Prader-Willi Syndrome - blood | Genetic Diseases, Inborn - immunology | Austria - epidemiology | Down Syndrome - epidemiology | Turner Syndrome - immunology | Germany - epidemiology | Down Syndrome - immunology | Diabetic Retinopathy - epidemiology | Dyslipidemias - epidemiology | Adolescent | Diabetic Nephropathies - epidemiology | Genetic Diseases, Inborn - physiopathology | Longitudinal Studies | Index Medicus
Journal Article