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NIPT-based prenatal screening of maternal Xq28 copy number variations in a cohort of 80371 pregnancies

2026-05-12

Abstract excerpt

<title>Abstract</title> <p>Purpose Copy number variation (CNVs) can result in various genomic diseases and variable clinical phenotypes. This study aimed to assess the feasibility and reliability of noninvasive prenatal testing (NIPT) for prenatal screening of maternal copy number variation (CNVs) involving Xq28 recurrent region. Methods In this retrospective, single-center study, we analyzed the NIPT data of 8...

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Literature Corpus work
c8cf5510-024d-58a1-bc88-0b8c6c98ecd7
DOI
10.21203/rs.3.rs-9297386/v1
Open publication

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NIPT-based prenatal screening of maternal Xq28 copy number variations in a cohort of 80371 pregnanciesDOI 10.21203/rs.3.rs-9297386/v1
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