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Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing

21 May 2018

Abstract excerpt

A prospective analysis investigating the associations between pathogenic copy number variations (pCNVs) and ultrasound soft markers (USMs) in fetuses and evaluating the clinical value of copy number variation sequencing (CNV-seq) in such pregnancy studies was carried out. 3,398 unrelated Chinese women with singleton pregnancies and undergone amniocentesis at 18-36 weeks of gestation for fetal CNV-seq were...

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Share to Fetal and Pediatric Neurological Disorders
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PMID: 29802277
DOI: 10.1038/s41598-018-26555-6

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