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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:J Int Med Res
Autors principals: Zhang, Rui, Chen, Xiangbin, Wang, Dong, Chen, Xuan, Wang, Chao, Zhang, Yuhong, Xu, Mengnan, Yu, Jingcui
Format: Artigo
Idioma:Inglês
Publicat: SAGE Publications 2019
Matèries:
Clinical Research Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6421393/
https://ncbi.nlm.nih.gov/pubmed/30732499
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0300060518818020
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars