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Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations

Johanna Winberg1,2, Peter Gustavsson1,2, Ellika Sahlin1,2

  • 1Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

Molecular Genetics & Genomic Medicine
|December 15, 2019
PubMed
Abstract

Keywords:
anorectal malformationsarray-CGHcopy number variationesophageal atresiahydronephrosismosaicism

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