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What is Genetic Study of Neurodevelopmental Disorders about?

The study investigates genetic alterations in a cohort of 1125 Italian children and adolescents with neurodevelopmental disorders using array comparative genomic hybridization (a-CGH). It identifies significant copy number variants (CNVs) and variants of uncertain significance (VOUS) in genes potentially linked to these disorders. The findings emphasize the diagnostic value of a-CGH as a routine genetic test for uncovering molecular alterations associated with neurodevelopmental conditions.

Author

Noemi Falcone

Language

EN