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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Egile Nagusiak: Yi-Fang Dai (Egilea), Xiao-Qing Wu (Egilea), Hai-Long Huang (Egilea), Shu-Qiong He (Egilea), Dan-Hua Guo (Egilea), Ying Li (Egilea), Na Lin (Egilea), Liang-Pu Xu (Egilea)
Formatua: Liburua
Argitaratua: BMC, 2024-01-01T00:00:00Z.
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