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Updated: Aug 10, 2025

Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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22q11 Copy Number Variations in a Brazilian Cohort of Children with Congenital Heart Disorders

Maiara A Floriani1, Andressa S Santos2, Bruna L Diniz1

  • 1Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil.

Molecular Syndromology
|February 13, 2023
PubMed
Abstract

Keywords:
22q11.2 deletion syndromeCongenital heart diseaseDNA Copy number variationMultiplex ligation-dependent probe amplification

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