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2011, Genetic syndromes and communication disorders series, ISBN 9781597563499, xxiii, 381
Book
American Journal of Psychiatry, ISSN 0002-953X, 06/2014, Volume 171, Issue 6, pp. 627 - 639
Journal Article
2008, Genetic syndromes and communication disorders series, ISBN 9781597560719, Volume 1, x, 279
Book
Journal of Intellectual Disability Research, ISSN 0964-2633, 04/2015, Volume 59, Issue 4, pp. 307 - 318
BackgroundThere are a number of neurogenetic syndromes with well described behavioural phenotypes including fragile X syndrome, Prader-Willi syndrome, Williams... 
ADHD | ASD | VCFS | syndrome | velo‐cardio‐facial syndrome | fragile | Prader–Willi syndrome | autism spectrum disorder | Williams syndrome | Velo-cardio-facial syndrome (VCFS) | Fragile X syndrome | Autism spectrum disorder (ASD) | Prader-Willi syndrome | CONTROLLED-TRIAL | DEFICIT HYPERACTIVITY DISORDER | fragile X syndrome | velo-cardio-facial syndrome (VCFS) | 22Q11.2 DELETION SYNDROME | AUTISM SPECTRUM DISORDERS | PERVASIVE DEVELOPMENTAL DISORDERS | EDUCATION, SPECIAL | FRAGILE-X-SYNDROME | PSYCHIATRIC-DISORDERS | VELOCARDIOFACIAL SYNDROME | REHABILITATION | autism spectrum disorder (ASD) | PRADER-WILLI-SYNDROME | YOUNG-CHILDREN | Humans | Parents | Child, Preschool | Male | Fragile X Syndrome - drug therapy | Young Adult | Ireland | Adult | Female | Attention Deficit Disorder with Hyperactivity - diagnosis | Mental Disorders - diagnosis | Child | Autism Spectrum Disorder - diagnosis | DiGeorge Syndrome - drug therapy | Prader-Willi Syndrome - drug therapy | Health Care Surveys - methods | Prader-Willi Syndrome - diagnosis | Williams Syndrome - drug therapy | United Kingdom | Attention Deficit Disorder with Hyperactivity - drug therapy | Syndrome | Williams Syndrome - diagnosis | DiGeorge Syndrome - diagnosis | Mental Disorders - drug therapy | Psychopharmacology | Adolescent | Autism Spectrum Disorder - drug therapy | Health Care Surveys - statistics & numerical data | Fragile X Syndrome - diagnosis | Psychological aspects | Surveys | Health aspects | Mental health | Attention-deficit hyperactivity disorder | Attention deficit disorder | Disabled children | Mental disorders | Hyperactivity
Journal Article
Journal of Intellectual Disability Research, ISSN 0964-2633, 10/2012, Volume 56, Issue 10, pp. 929 - 946
Background  A number of genetic conditions with associated intellectual disability and/or special educational needs have increasingly well‐defined behavioural... 
behavioural phenotypes | VCFS | Down syndrome | Prader–Willi syndrome | fragile X | Williams syndrome | Behavioural phenotypes | Prader-Willi syndrome | Fragile X | DEFICIT HYPERACTIVITY DISORDER | 22Q11.2 DELETION SYNDROME | AUTISM SPECTRUM DISORDERS | EDUCATION, SPECIAL | DOWN-SYNDROME | FRAGILE-X-SYNDROME | VELOCARDIOFACIAL SYNDROME | PSYCHIATRIC-DISORDERS | REHABILITATION | MENTAL-RETARDATION SYNDROMES | PRADER-WILLI-SYNDROME | CARDIO-FACIAL SYNDROME | Intervention | Student Needs | Behavior Modification | Mental Retardation | Cognitive Restructuring | Genetic Disorders | Guidelines | Special Education | Down Syndrome | Special Needs Students | Etiology | Behavior Problems | Genetics | Educational Needs | Teaching Methods | Symptoms (Individual Disorders) | Social Behavior Disorders - genetics | Williams Syndrome - complications | Williams Syndrome - genetics | Humans | Intellectual Disability - complications | Prader-Willi Syndrome - complications | Williams Syndrome - psychology | Intellectual Disability - genetics | Prader-Willi Syndrome - psychology | Students - psychology | Social Behavior Disorders - psychology | DiGeorge Syndrome - complications | Down Syndrome - complications | Prader-Willi Syndrome - genetics | Child | DiGeorge Syndrome - genetics | Fragile X Syndrome - genetics | Child Behavior Disorders - psychology | Education of Intellectually Disabled - methods | DiGeorge Syndrome - psychology | Fragile X Syndrome - complications | Child Behavior Disorders - etiology | Phenotype | Social Behavior Disorders - etiology | Fragile X Syndrome - psychology | Down Syndrome - genetics | Intellectual Disability - psychology | Child Behavior Disorders - genetics | School Health Services | Down Syndrome - psychology | Teachers | Genetic disorders | Analysis | Genetic aspects | Genotype & phenotype | Learning disabilities | Behavior modification | Special education
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 1/2012, Volume 69, Issue 1, pp. 17 - 27
Chromosome 22q11 deletion is the most common chromosomal deletion syndrome and is found in the majority of patients with DiGeorge syndrome and... 
Life Sciences | Biochemistry, general | Autoimmunity | Life Sciences, general | DiGeorge syndrome | Velo-cardio-facial syndrome | CHARGE syndrome | 22q11 deletion | Biomedicine general | Cell Biology | SEVERE COMBINED IMMUNODEFICIENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | DIGEORGE-SYNDROME/VELOCARDIOFACIAL SYNDROME | JUVENILE RHEUMATOID-ARTHRITIS | LIVE VIRAL VACCINES | 10P DELETION | T-CELL DEVELOPMENT | SYNDROME VELOCARDIOFACIAL SYNDROME | THYMUS TRANSPLANTATION | CARDIO-FACIAL SYNDROME | Chromosome Deletion | Central Tolerance | Humans | Autoimmune Diseases - immunology | Abnormalities, Multiple - immunology | CHARGE Syndrome - immunology | DiGeorge Syndrome - immunology | Autoimmune Diseases - genetics | Chromosomes, Human, Pair 22 - genetics | T-Lymphocytes - metabolism | Chromosomes, Human, Pair 22 - immunology | Thymus Gland - pathology | Immunologic Deficiency Syndromes - genetics | T-Lymphocytes - immunology | Thymus Gland - growth & development | Thymus Gland - immunology | CHARGE Syndrome - genetics | Immunologic Deficiency Syndromes - immunology | Abnormalities, Multiple - genetics | DiGeorge Syndrome - genetics | T cells | Health aspects | Immunodeficiency | Chromosomes | Immunology | Heart | Recurrent infection | Chromosome deletion | Lymphocytes T | Immunological tolerance | Thymus | Immunological aspects | speech | chromosome 22 | Thymic hypoplasia | Children
Journal Article
Immunological Reviews, ISSN 0105-2896, 01/2019, Volume 287, Issue 1, pp. 186 - 201
Journal Article