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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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Detalles Bibliográficos
Autores principales:	Zhang, Jinman, Tang, Xinhua, Hu, Jilin, He, Guilin, Wang, Jian, Zhu, Yingting, Zhu, Baosheng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2021
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265053/ https://www.ncbi.nlm.nih.gov/pubmed/34238233 http://dx.doi.org/10.1186/s12884-021-03918-y

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