Contribution of chromosomal abnormalities at 10q and 22q to autism / Nagwa A. MEGUID in Research in Autism Spectrum Disorders, 50 (June 2018)  

Public ISBD [article]  inResearch in Autism Spectrum Disorders > 50 (June 2018) . - p.43-50 Titre : Contribution of chromosomal abnormalities at 10q and 22q to autism Type de document : Texte imprimé et/ou numérique Auteurs : Nagwa A. MEGUID, Auteur ; Maha M. EID, Auteur ; Amal M. MOHAMED, Auteur ; Heba GHANOUM, Auteur ; Nivine A. HELMY, Auteur ; Ola M. EID, Auteur Année de publication : 2018 Article en page(s) : p.43-50 Langues : Anglais (eng) Mots-clés : Autism  Chromosomal abnormalities  Chromosome 10q  Chromosome 22q Index. décimale : PER Périodiques Résumé : Autism’s etiology is heterogeneous. It derives generically from a complex of interactions between genetic, epigenetic and environmental factors. Chromosomal rearrangements at almost all chromosomes have been reported among individuals with autism spectrum disorders (ASD). In this report, we represent three autistic patients with chromosomal abnormalities at 10q and 22q with an interesting case of 10q duplication rather than deletion. This report explores the contribution of the affected genomic regions to ASD. It may contribute to the field of research categorizing candidate loci for ASD, which would be useful in genotype– phenotype analyses for ASD. En ligne : https://doi.org/10.1016/j.rasd.2018.03.003 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=356 [article] Contribution of chromosomal abnormalities at 10q and 22q to autism [Texte imprimé et/ou numérique] / Nagwa A. MEGUID, Auteur ; Maha M. EID, Auteur ; Amal M. MOHAMED, Auteur ; Heba GHANOUM, Auteur ; Nivine A. HELMY, Auteur ; Ola M. EID, Auteur . - 2018 . - p.43-50. Langues : Anglais (eng) in Research in Autism Spectrum Disorders > 50 (June 2018) . - p.43-50 Mots-clés : Autism  Chromosomal abnormalities  Chromosome 10q  Chromosome 22q Index. décimale : PER Périodiques Résumé : Autism’s etiology is heterogeneous. It derives generically from a complex of interactions between genetic, epigenetic and environmental factors. Chromosomal rearrangements at almost all chromosomes have been reported among individuals with autism spectrum disorders (ASD). In this report, we represent three autistic patients with chromosomal abnormalities at 10q and 22q with an interesting case of 10q duplication rather than deletion. This report explores the contribution of the affected genomic regions to ASD. It may contribute to the field of research categorizing candidate loci for ASD, which would be useful in genotype– phenotype analyses for ASD. En ligne : https://doi.org/10.1016/j.rasd.2018.03.003 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=356

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