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Clinical Findings and Genetic Analysis of Patients with Copy Number Variants Involving 17p13.3 By Using a Single Nucleotide Polymorphism Array: A Single-Center Experience

2022-08-02

Abstract excerpt

<h4>Background: </h4> 17p13.3 microdeletions or microduplications (collectively known as copy number variants or CNVs) have been described in association with individuals with neurodevelopmental disorders. While, studies on 17p13.3 CNVs in prenatal diagnosis are limited. This study aims to investigate the clinical significance of 17p13.3 CNVs with varied size and gene contents in prenatal and postnatal samples. Me...

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Literature Corpus work: 734df133-f493-557b-9271-8f208b5e6d13
DOI: 10.21203/rs.3.rs-1839465/v1

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