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Brain & Development, ISSN 0387-7604, 2013, Volume 36, Issue 8, pp. 725 - 729
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2013, Volume 21, Issue 12, pp. 1349 - 1355
Journal Article
Brain & Development, ISSN 0387-7604, 2011, Volume 34, Issue 7, pp. 601 - 604
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 05/2013, Volume 21, Issue 5, pp. 522 - 527
Journal Article
Genetics in Medicine, ISSN 1098-3600, 01/2018, Volume 20, Issue 1, pp. 98 - 108
Journal Article
BMC PEDIATRICS, ISSN 1471-2431, 10/2018, Volume 18, Issue 1, pp. 333 - 15
Background: Rett Syndrome (RTT) is a complex neurodevelopmental disorder, frequently associated with epilepsy. Despite increasing recognition of the clinical... 
MeCP2 | ERP | CDKL5 | AUTISM | EEG | Rett syndrome | Network | DISORDER | PEDIATRICS | Physiological aspects | Electroencephalography | Genetic aspects | Research | Varieties | Electrodes | Autism | Asymmetry | Epilepsy | Biomarkers | Connectivity | Nervous system | Mutation | Quantitative analysis
Journal Article
REVISTA DE NEUROLOGIA, ISSN 0210-0010, 05/2011, Volume 52, Issue 10, pp. 597 - 602
Journal Article
Revista de Neurologia, ISSN 0210-0010, 2011, Volume 52, Issue 10, pp. 597 - 602
Journal Article
JOURNAL OF MEDICAL GENETICS, ISSN 0022-2593, 04/1999, Volume 36, Issue 4, pp. 343 - 345
A girl fulfilling four/five of six inclusion criteria and eight/nine of 11 supportive criteria for atypical Rett syndrome had a cytogenetic deletion of... 
HYBRIDIZATION | deletion | chromosome 3 | Rett syndrome | GENETICS & HEREDITY | Gene Deletion | Humans | Female | In Situ Hybridization, Fluorescence | Chromosome Mapping | Rett Syndrome - genetics | Child | Chromosomes, Human, Pair 3 - genetics | Deletion | Chromosome 3 | Congenital diseases | Chromosomes | Girls | Deoxyribonucleic acid--DNA | Short Report
Journal Article