Prevalence of chromosomal abnormalities identified by copy number variation sequencing in high-risk pregnancies, spontaneous abortions, and suspected genetic disorders

OBJECTIVE: High-throughput sequencing based on copy number variation (CNV-seq) is commonly used to detect chromosomal abnormalities including aneuploidy. This study provides evidence for the prevalence of chromosomal abnormalities in target populations. METHODS: A total of 160 samples, including 83...

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Detalles Bibliográficos
Autores principales: Zhang, Rui, Chen, Xiangbin, Wang, Dong, Chen, Xuan, Wang, Chao, Zhang, Yuhong, Xu, Mengnan, Yu, Jingcui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Clinical Research Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421393/
https://www.ncbi.nlm.nih.gov/pubmed/30732499
http://dx.doi.org/10.1177/0300060518818020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421393/
https://www.ncbi.nlm.nih.gov/pubmed/30732499
http://dx.doi.org/10.1177/0300060518818020

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