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

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 microduplication...

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Publicado no:Noro Psikiyatr Ars
Main Authors: Görker, Işık, Gürkan, Hakan, Ulusal, Selma, Atli, Engin, Ayaz, Güçlü, Ceylan, Cansın, Tozkir, Hilmi, Altay, Mengühan Araz, Erol, Ali, Yildiz, Nazike, Direk, Ceren, Akköprü, Hilal, Kilit, Neriman, Aykutlu, Hasan Cem, Bozatli, Leyla, Çelik, Zeki, Berberoğlu, Kıvanç Kudret
Formato: Artigo
Idioma:Inglês
Publicado em: Noro-Psikiyatri Arsivi 2018
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6138224/
https://ncbi.nlm.nih.gov/pubmed/30224866
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/npa.2017.21611
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