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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Materyal Türü: | Kitap |
Baskı/Yayın Bilgisi: |
BMC,
2024-01-01T00:00:00Z.
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Yer Numarası: |
A1234.567 |
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Kopya Bilgisi 1 | Kütüphanede |