Genetic tests aid in counseling of fetuses with cerebellar vermis defects-Reference-Cited by-同舟云学术

Genetic tests aid in counseling of fetuses with cerebellar vermis defects

Published:2020-05-28 Issue:10 Volume:40 Page:1228-1238
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Li Lushan¹^ORCID,Fu Fang¹,Li Ru²,Xiao Weiqiang³,Yu Qiuxia²^ORCID,Wang Dan²,Jing Xiangyi²^ORCID,Zhang Yongning²,Yang Xin¹,Pan Min¹,Liu Zequn¹,Liao Can¹^ORCID

Affiliation:

1. Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

2. Eugenic and Perinatal Institute, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

3. Radiation department, Guangzhou Women and Children's Medical Center Guangzhou Medical University Guangzhou China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5732

Reference37 articles.

1. Cell number and cell density in the cerebellar cortex of man and some other mammals

2. Surface-Based Atlases of Cerebellar Cortex in the Human, Macaque, and Mouse

3. Congenital hypoplasia of the cerebellum: developmental causes and behavioral consequences

4. The Fetal Cerebellar Vermis

5. Cellular and molecular basis of cerebellar development

Cited by 18 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Optimal prenatal genetic diagnostic approach for posterior fossa malformation: karyotyping, copy number variant testing, or whole-exome sequencing?;European Journal of Medical Research;2024-07-31

2. Advancing fetal diagnosis and prognostication using comprehensive prenatal phenotyping and genetic testing;Pediatric Research;2024-06-27

3. Prenatal Genome-Wide Sequencing analysis (Exome or Genome) in detecting pathogenic Single Nucleotide Variants in fetal Central Nervous System Anomalies: systematic review and meta-analysis;European Journal of Human Genetics;2024-03-15

4. Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis;Prenatal Diagnosis;2023-12-06

5. Diagnostic yield of prenatal exome sequencing in the genetic screening of fetuses with brain anomalies detected by MRI and ultrasonography: A systematic review and meta‐analysis;BJOG: An International Journal of Obstetrics & Gynaecology;2023-11-06