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Updated: Mar 31, 2026

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

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Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of

Fátima Torres1, Mafalda Barbosa2, Patrícia Maciel3

  • 1CGC Genetics, Porto, Portugal Instituto de Ciências Biomédicas Abel Salazar, Universidade do Porto, Porto, Portugal.

Journal of Medical Genetics
|October 28, 2015
PubMed

Keywords:
Autism, EpilepsyCNVs, Risk factorsGenetic counselingNeurodevelopmental disordersSchizophrenia, Mood disorders

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