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Identification of copy number variants in children and adolescents with autism spectrum disorder: a study from Turkey.

Molecular biology reports - 1 Nov 2021

Özaslan Ahmet, Kayhan Gülsüm, İşeri Elvan, Ergün Mehmet Ali, Güney Esra, Perçin Ferda Emriye

Abstract excerpt

BACKGROUND: Copy number variants (CNVs) play a key role in the etiology of autism spectrum disorder (ASD). Therefore, recent guidelines recommend chromosomal microarrays (CMAs) as first-tier genetic tests. This study's first aim was to determine the clinical usefulness of CMAs in children diagnosed with ASD in a Turkish population. The second aim was to describe the CNVs and clinical phenotypes of children with...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 34637094
DOI: 10.1007/s11033-021-06745-8

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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