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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
Journal Article
1995, Language of science, ISBN 9780306450556
eBook
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
Cellular and Molecular Life Sciences, ISSN 1420-682X, 5/2013, Volume 70, Issue 9, pp. 1543 - 1573
Epigenetic mechanisms play an important role in gene regulation during development. DNA methylation, which is probably the most important and best-studied... 
Life Sciences | Biochemistry, general | Life Sciences, general | Disease | Epigenetics | Mutation | Biomedicine general | Cell Biology | SYSTEMIC-LUPUS-ERYTHEMATOSUS | RUBINSTEIN-TAYBI-SYNDROME | BIOCHEMISTRY & MOLECULAR BIOLOGY | S-ADENOSYLMETHIONINE SYNTHETASE | CPG-BINDING-PROTEIN | XNP/ATR-X GENE | METHIONINE ADENOSYLTRANSFERASE 1A | CELL BIOLOGY | FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY | COFFIN-LOWRY-SYNDROME | SINGLE NUCLEOTIDE POLYMORPHISM | GLYCINE N-METHYLTRANSFERASE | Coffin-Lowry Syndrome - genetics | Neoplasms - metabolism | Epigenesis, Genetic | Humans | Lupus Erythematosus, Systemic - metabolism | Muscular Dystrophy, Facioscapulohumeral - genetics | alpha-Thalassemia - metabolism | DNA Methylation | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - genetics | Neoplasms - genetics | Sotos Syndrome - metabolism | Coffin-Lowry Syndrome - metabolism | alpha-Thalassemia - genetics | Muscular Dystrophy, Facioscapulohumeral - metabolism | Sotos Syndrome - genetics | DNA Modification Methylases - metabolism | Cockayne Syndrome - metabolism | DNA - metabolism | Rubinstein-Taybi Syndrome - metabolism | DNA - genetics | Rett Syndrome - metabolism | DNA Modification Methylases - genetics | Animals | Histones - genetics | CHARGE Syndrome - metabolism | Lupus Erythematosus, Systemic - genetics | Cockayne Syndrome - genetics | CHARGE Syndrome - genetics | Histones - metabolism | Rett Syndrome - genetics | Mental Retardation, X-Linked - metabolism | Liver cancer | Gene mutations | Genes | Transferases | Immunodeficiency | Physiological aspects | Methylation | Glycine | Mental illness | S-adenosylmethionine | CHARGE syndrome
Journal Article