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Article

Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.

Journal of autism and developmental disorders - 1 Feb 2018

Napoli Eleonora, Russo Serena, Casula Laura, Alesi Viola, Amendola Filomena Alessandra, Angioni Adriano, Novelli Antonio, Valeri Giovanni, Menghini Deny, Vicari Stefano

Abstract excerpt

Copy-number variants (CNVs) are associated with susceptibility to autism spectrum disorder (ASD). To detect the presence of CNVs, we conducted an array-comparative genomic hybridization (array-CGH) analysis in 133 children with "essential" ASD phenotype. Genetic analyses documented that 12 children had causative CNVs (C-CNVs), 29 children had non-causative CNVs (NC-CNVs) and 92 children without CNVs (W-CNVs)....

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Source

Identifiers

PMID: 29027068
DOI: 10.1007/s10803-017-3329-4

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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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