Integrated CNV-seq, karyotyping and SNP-array analyses for effective prenatal diagnosis of chromosomal mosaicism

Abstract Background Emerging studies suggest that low‐coverage massively parallel copy number variation sequencing (CNV-seq) more sensitive than chromosomal microarray analysis (CMA) for detecting low-level mosaicism. However, a retrospective back-to-back comparison evaluating accuracy, efficacy, an...

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Váldodahkkit: Na Ma (Dahkki), Hui Xi (Dahkki), Jing Chen (Dahkki), Ying Peng (Dahkki), Zhengjun Jia (Dahkki), Shuting Yang (Dahkki), Jiancheng Hu (Dahkki), Jialun Pang (Dahkki), Yanan Zhang (Dahkki), Rong Hu (Dahkki), Hua Wang (Dahkki), Jing Liu (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: BMC, 2021-02-01T00:00:00Z.
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3rd Floor Main Library

oažžasuvvan: 3rd Floor Main Library
Hildobáiki: A1234.567
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