Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two cases

Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two cases

Chromosomal mosaicism remains a perpetual diagnostic and clinical dilemma. In the present study, we detected two prenatal trisomy 9 mosaic syndrome cases by using multiple genetic testing methods. The non-invasive prenatal testing (NIPT) results suggested trisomy 9 in two fetuses. Karyotype analysis...

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Bibliographic Details
Main Authors: Na Ma, Zhenhua Zhu, Jiancheng Hu, Jialun Pang, Shuting Yang, Jing Liu, Jing Chen, Wanglan Tang, Haiyan Kuang, Rong Hu, Zhuo Li, Hua Wang, Ying Peng, Hui Xi
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-03-01
Series:Frontiers in Genetics
Subjects:
karyotype
copy number variation sequencing
non-invasive prenatal testing
chromosomal microarray analysis
mosaicism
trisomy 9
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2023.1121121/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2023.1121121/full

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