Investigation of Copy Number Variation by arrayCGH in Turkish Children and Adolescents Diagnosed with Autism Spectrum Disorders

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GÖRKER I., GÜRKAN H., Ulusal S., ATLI E., Ayaz G., Ceylan C., ...More

NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, vol.55, no.3, pp.215-219, 2018 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 55 Issue: 3
• Publication Date: 2018
• Doi Number: 10.5152/npa.2017.21611
• Journal Name: NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
• Page Numbers: pp.215-219
• Eskisehir Osmangazi University Affiliated: Yes

Abstract

Aim: The development of whole-genome screening methodologies for the detection of copy number variations (CNVs), such as array-based comparative genomic hybridization (aCHG), provides a much higher resolution than karyotyping leading to the identification of novel microdeletion and microduptication syndromes often associated with an autism spectrum disease (ASD) phenotype. The aim of the study was to determine CNVs of patients with ASD by using array-based comparative genomic hybridization.