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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...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
PeerJ Inc.
2022
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| Materias: | |
| 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 |