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Article

Evaluation and management of DMD gene copy number variations detected by prenatal SNP-array testing.

BMC medical genomics - 6 Mar 2026

Hu Jiancheng, Pang Jialun, Hu Rong, Zhou Lin, Yu Wenxian, Xi Hui, Luo Yingchun, Yang Shuting, Tang Wanglan, Hu Ai, Chen Jing, Peng Ying

Abstract excerpt

OBJECTIVE: This study aims to evaluate the clinical management of incidental findings of copy number variations (CNVs) in the DMD gene detected through prenatal single nucleotide polymorphism array (SNP-array). METHODS: Prenatal SNP-array testing was performed on samples exhibiting CNVs in the DMD locus, followed by parental analysis using the same technique. Additionally, multiplex ligation-dependent probe...

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Share to DNA Copy Number Variations
Share to Dystrophin

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DMD gene

Share to Muscular Dystrophy, Duchenne

Share to Oligonucleotide Array Sequence Analysis

Share to Polymorphism, Single Nucleotide

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Source

Open in PubMed Open full text

Identifiers

PMID: 41792804
DOI: 10.1186/s12920-026-02333-6
PMCID: PMC13088639

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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