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Sequential application of copy number variation sequencing and quantitative fluorescence polymerase chain reaction in genetic analysis of miscarriage and stillbirth

BACKGROUND: Copy number variation sequencing (CNV‐seq) could detect most chromosomal abnormalities except polyploidy, and quantitative fluorescence polymerase chain reaction (QF‐PCR) is a supplementary method to CNV‐seq in triploid detection. This study aimed to evaluate the feasibility of sequentia...

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Detalles Bibliográficos
Autores principales:	Chen, Quan, Zhang, Hao, Li, Xue, Li, Junxing, Chen, Huijuan, Liu, Lin, Zhou, Shijie, Xu, Zhihong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10422063/ https://www.ncbi.nlm.nih.gov/pubmed/37073418 http://dx.doi.org/10.1002/mgg3.2187

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