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Journal of the American Academy of Child & Adolescent Psychiatry, ISSN 0890-8567, 2010, Volume 49, Issue 8, pp. 794 - 809
.... Results Several genetic syndromes... 
Pediatrics | Psychiatry | autism spectrum disorders | epigenetics | genetics | DNA METHYLATION | PSYCHIATRY | PSYCHOLOGY, DEVELOPMENTAL | NEUROTROPHIC FACTOR BDNF | ANGELMAN-SYNDROME | UNIPARENTAL DISOMY | SEROTONIN TRANSPORTER GENE | RECEPTOR OXTR GENE | BECKWITH-WIEDEMANN-SYNDROME | FRAGILE-X-SYNDROME | LINKAGE-DISEQUILIBRIUM | PEDIATRICS | 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 of intellectual disability research, ISSN 0964-2633, 1992
Journal
American journal on mental retardation, ISSN 0895-8017, 1987
Journal
Journal
2017, Clinics in developmental medicine (unnumbered), ISBN 9781909962835, xxv, 225 pages
Book
British journal of learning disabilities, ISSN 1354-4187
Journal
Clinical Genetics, ISSN 0009-9163, 08/2003, Volume 64, Issue 2, pp. 83 - 95
Ausió J, Levin DB, de Amorim GV, Bakker S and Macleod PM. Syndromes of disordered chromatin remodeling... 
Rubinstein–Taybi syndrome | thalassemia | Coffin–Lowry syndrome | Rett syndrome | X-linked | chromatin remodeling | histone postranslational modifications | immunodeficiency–centromeric instability–facial anomalies syndrome | chromatin | mental retardation syndrome | α‐thalassemia | Coffin–Lowry syndrome | X‐linked | Rubinstein–Taybi syndrome | immunodeficiency–centromeric instability–facial anomalies syndrome | Centromeric instability-facial anomalies syndrome | Chromatin | Histone postranslational modifications | α-thalassemia/mental retardation syndrome, X-linked | Immunodeficiency | Rubinstein | Coffin-Lowry syndrome | Chromatin remodeling | Taybi syndrome | RUBINSTEIN-TAYBI-SYNDROME | DNA METHYLTRANSFERASE GENE | Rubinstein-Taybi syndrome | ALPHA-THALASSEMIA | ATR-X SYNDROME | alpha-thalassemia/mental retardation syndrome, X-linked | TRANSCRIPTIONAL COACTIVATOR CBP | CPG-BINDING PROTEIN-2 | HISTONE ACETYLATION | immunodeficiency-centromeric instability-facial anomalies syndrome | COFFIN-LOWRY-SYNDROME | MENTAL-RETARDATION SYNDROME | GENETICS & HEREDITY | RETT-SYNDROME MUTATIONS | Coffin-Lowry Syndrome - genetics | Rett Syndrome - complications | alpha-Thalassemia - complications | Mental Retardation, X-Linked - complications | Rett Syndrome - diagnosis | Humans | Genetic Diseases, Inborn - genetics | Chromatin Assembly and Disassembly - genetics | Coffin-Lowry Syndrome - complications | Mutation - genetics | Rubinstein-Taybi Syndrome - complications | Mutation - physiology | Mental Retardation, X-Linked - genetics | Rubinstein-Taybi Syndrome - diagnosis | Rubinstein-Taybi Syndrome - genetics | Mental Retardation, X-Linked - diagnosis | Genetic Diseases, Inborn - complications | alpha-Thalassemia - diagnosis | alpha-Thalassemia - genetics | Rett Syndrome - genetics | Genetic Diseases, Inborn - diagnosis | Chromatin Assembly and Disassembly - physiology | Coffin-Lowry Syndrome - diagnosis
Journal Article
International review of research in mental retardation, ISSN 0074-7750, 1966
Journal
Annals of neurology, ISSN 0364-5134, 2010, Volume 68, Issue 6, pp. 944 - 950
Objective Rett syndrome (RTT) is a severe neurodevelopmental disease that affects approximately 1 in 10,000 live female births and is often caused by mutations in Methyl‐CpG‐binding protein 2 (MECP2... 
CDKL5 MUTATIONS | MECP2 MUTATIONS | DISORDER | GIRLS | VARIANT | NEUROSCIENCES | CLINICAL NEUROLOGY | Animals | Rett Syndrome - diagnosis | Humans | Terminology as Topic | Mutation - genetics | Rett Syndrome - genetics | Methyl-CpG-Binding Protein 2 - genetics
Journal Article