Accuracy of expanded noninvasive prenatal testing for maternal copy number variations: A comparative study with CNV-seq of maternal lymphocyte DNA
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Publisher
Elsevier BV
Reference15 articles.
1. Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG);Dungan;Genet Med,2023
2. Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort;Su;Ultrasound Obstet Gynecol,2022
3. Clinical utility of expanded non-invasive prenatal screening and chromosomal microarray analysis in high-risk pregnancy;Zhu;Ultrasound Obstet Gynecol,2021
4. Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes;Liang;Genet Med,2019
5. Copy-number variation and false positive prenatal aneuploidy screening results;Snyder;N Engl J Med,2015
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