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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
Nature Genetics, ISSN 1061-4036, 07/2012, Volume 44, Issue 7, pp. 788 - 792
IMAGe syndrome (intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita and genital anomalies) is an undergrowth developmental... 
BECKWITH-WIEDEMANN-SYNDROME | GENE | UBIQUITIN | SEQUENCE | GENETICS & HEREDITY | DEPENDENT KINASE INHIBITOR | ADRENAL HYPOPLASIA | INHERITANCE | ASSOCIATION | P57(KIP2) | FAMILY | Cyclin-Dependent Kinase Inhibitor p57 - metabolism | Hypoadrenocorticism, Familial | Protein Binding - genetics | Cyclin-Dependent Kinase Inhibitor p57 - genetics | Exons | Humans | Fetal Growth Retardation - genetics | Male | Adrenal Hyperplasia, Congenital - genetics | Genetic Loci | Beckwith-Wiedemann Syndrome - genetics | Osteochondrodysplasias - genetics | Proliferating Cell Nuclear Antigen - genetics | HEK293 Cells | Female | Genetic Diseases, X-Linked - genetics | Genetic Predisposition to Disease | Drosophila | Adrenal Hyperplasia, Congenital - metabolism | Fetal Growth Retardation - metabolism | Protein Structure, Tertiary - genetics | Beckwith-Wiedemann Syndrome - metabolism | Genetic Diseases, X-Linked - metabolism | Adrenal Insufficiency | Animals | Chromosomes, Human, Pair 11 | Mutation | Proliferating Cell Nuclear Antigen - metabolism | Cell Line, Transformed | Osteochondrodysplasias - metabolism | Gene mutations | Fetus | Genetic aspects | Research | Health aspects | Growth retardation | Risk factors | Genes | Genomes | Experiments | Proteins | Design | Insects | Genetics | Genetic testing | Charitable foundations | Bioinformatics | Binding sites | Deoxyribonucleic acid--DNA
Journal Article
European journal of human genetics, ISSN 1018-4813, 2016, Volume 24, Issue 10, pp. 1377 - 1387
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 02/2016, Volume 74, Issue 2, pp. 231 - 231
There are a significant number of diseases and treatment considerations of considerable importance relating to the skin and renal systems. This emphasizes the... 
genetic | nephrology | dermatology | autoimmune | genodermatoses | inflammatory | nephrocutaneous | Uterine Neoplasms - therapy | Skin Diseases - genetics | Tuberous Sclerosis - complications | Beckwith-Wiedemann Syndrome - therapy | Fabry Disease - genetics | Humans | Genetic Diseases, Inborn - genetics | von Hippel-Lindau Disease - complications | Genetic Diseases, Inborn - therapy | Beckwith-Wiedemann Syndrome - genetics | Kidney Diseases - genetics | Nail-Patella Syndrome - therapy | Neurofibromatosis 1 - therapy | Neoplastic Syndromes, Hereditary | Beckwith-Wiedemann Syndrome - complications | Leiomyomatosis - complications | Leiomyomatosis - therapy | Birt-Hogg-Dube Syndrome - complications | Turner Syndrome - complications | Turner Syndrome - therapy | Neurofibromatosis 1 - genetics | Uterine Neoplasms - genetics | von Hippel-Lindau Disease - therapy | Hamartoma Syndrome, Multiple - genetics | Skin Neoplasms - therapy | Nail-Patella Syndrome - genetics | Fabry Disease - complications | von Hippel-Lindau Disease - genetics | Hamartoma Syndrome, Multiple - complications | Birt-Hogg-Dube Syndrome - genetics | Tuberous Sclerosis - genetics | Tuberous Sclerosis - therapy | Skin Neoplasms - complications | Birt-Hogg-Dube Syndrome - therapy | Hamartoma Syndrome, Multiple - therapy | Skin Neoplasms - genetics | Neurofibromatosis 1 - complications | Uterine Neoplasms - complications | Nail-Patella Syndrome - complications | Turner Syndrome - genetics | Fabry Disease - therapy | Mutation | Leiomyomatosis - genetics
Journal Article
PLoS Genetics, ISSN 1553-7390, 03/2009, Volume 5, Issue 3, pp. e1000423 - e1000423
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1/2012, Volume 21, Issue 1, pp. 10 - 25
Journal Article
Pediatric Clinics of North America, ISSN 0031-3955, 2015, Volume 62, Issue 2, pp. 411 - 426
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 02/2016, Volume 24, Issue 2, pp. 183 - 190
Journal Article