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Investigation on combined copy number variation sequencing and cytogenetic karyotyping for prenatal diagnosis
BACKGROUND: We aimed to evaluate the clinical value of copy number variation-sequencing (CNV-Seq) in combination with cytogenetic karyotyping in prenatal diagnosis. METHODS: CNV-Seq and cytogenetic karyotyping were performed in parallel for 9452 prenatal samples for comparison of the diagnostic perf...
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| Publicado no: | BMC Pregnancy Childbirth |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8265053/ https://ncbi.nlm.nih.gov/pubmed/34238233 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12884-021-03918-y |
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