Combined use of karyotyping and copy number variation sequencing technology in prenatal diagnosis

BACKGROUND: Karyotyping and genome copy number variation sequencing (CNV-seq) are two techniques frequently used in prenatal diagnosis. This study aimed to explore the diagnostic potential of using a combination of these two methods in order to provide a more accurate clinical basis for prenatal dia...

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Detalles Bibliográficos
Autores principales: Zhang, Suhua, Xu, Yuexin, Lu, Dan, Fu, Dan, Zhao, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Biochemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745786/
https://www.ncbi.nlm.nih.gov/pubmed/36523456
http://dx.doi.org/10.7717/peerj.14400

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9745786/
https://www.ncbi.nlm.nih.gov/pubmed/36523456
http://dx.doi.org/10.7717/peerj.14400

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