Experience of copy number variation sequencing applied in spontaneous abortion
Abstract Purpose We evaluated the value of copy number variation sequencing (CNV-seq) and quantitative fluorescence (QF)-PCR for analyzing chromosomal abnormalities (CA) in spontaneous abortion specimens. Methods A total of 650 products of conception (POCs) were collected from spontaneous abortion b...
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BMC,
2024-01-01T00:00:00Z.
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