Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities
GS demonstrates its feasibility in providing genetic diagnosis for foetal CNS abnormalities and shows the potential to expand the application to foetuses with other ultrasound anomalies in prenatal diagnosis.
Authors
- Zhi Gao (ORCID: https://orcid.org/0000-0002-1898-5309)
- Jinna Jiang
- Kwong Wai Choy (ORCID: https://orcid.org/0000-0002-3616-6200)
- Xiangdong Kong (ORCID: https://orcid.org/0000-0003-0030-7638)
- Ye Cao (ORCID: https://orcid.org/0000-0002-5712-1968)
- Meimei Liu (ORCID: https://orcid.org/0000-0003-1440-4754)
- Yuting Zheng (ORCID: https://orcid.org/0000-0002-2326-9067)
- Y Wang (ORCID: https://orcid.org/0000-0002-3643-6311)
- Xiaofan Zhu (ORCID: https://orcid.org/0000-0002-7303-1700)
- Zirui Dong (ORCID: https://orcid.org/0000-0002-3626-6500)
- Chunxiao Hua
Institutions
- Harbin Medical University (CN)
- Chinese University of Hong Kong (HK)
- First Affiliated Hospital of Xiamen University (CN)
- Chinese University of Hong Kong, Shenzhen (CN)
- First Affiliated Hospital of Zhengzhou University (CN)
Publication Details
- Journal
- Annals of Medicine
- Published
- 2024-09-06
- DOI
- https://doi.org/10.1080/07853890.2024.2399317
- Citations
- 4
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 2.20