Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities-Reference-Cited by-同舟云学术

Detection of genomic variants by genome sequencing in foetuses with central nervous system abnormalities

Published:2024-09-06 Issue:1 Volume:56 Page:
ISSN:0785-3890
Container-title:Annals of Medicine
language:en
Short-container-title:Annals of Medicine

Author:

Wang Yanfei¹,Liu Meimei²,Gao Zhi¹,Hua Chunxiao¹,Jiang Jinna³,Zheng Yuting⁴⁵,Dong Zirui⁴⁵,Cao Ye⁴⁵,Choy Kwong Wai⁴⁵,Zhu Xiaofan¹,Kong Xiangdong¹

Affiliation:

1. Genetics and Prenatal Diagnosis Center, Department of Obstetrics and Gynecology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

2. Prenatal Diagnosis Center, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, China

3. Department of Obstetrics and Gynecology, The First Affiliated Hospital of Xiamen University, Xiamen, China

4. Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong, Hong Kong, China

5. Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China

Funder

Key Scientific Research Project of Henan Province Colleges and Universities

Guangxi Key Laboratory of birth defects open project

Henan Province Medical Science and Technology Research Joint Project

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/07853890.2024.2399317

Reference45 articles.

1. Role of magnetic resonance imaging in fetuses with mild or moderate ventriculomegaly in the era of fetal neurosonography: systematic review and meta‐analysis

2. The challenge of imaging the fetal central nervous system: an aid to prenatal diagnosis, management and prognosis

3. Prenatal diagnosis of central nervous system abnormalities: Neurosonography versus fetal magnetic resonance imaging

4. Retrospective Assessment of Cost Savings From Prevention

5. Evaluation of Fetal Central Nervous System Anomalies by Ultrasound and Its Anatomical Co-relation