Application of expanded noninvasive prenatal test in prenatal diagnosis of fetuses with increased nuchal translucency
Author:
Affiliation:
1. Medical School of Chinese PLA, Chinese PLA General hospital, Beijing, China
2. Chinese PLA General hospital, Beijing, China
Funder
Genetic disease of birth defects in military families of child-bearing age
Establishment and application of prenatal screening and prenatal diagnosis database
Publisher
Informa UK Limited
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2021.1909564
Reference28 articles.
1. Abnormal nuchal translucency: residual risk with normal cell-free DNA screening
2. Should cell‐free DNA testing be used in pregnancy with increased fetal nuchal translucency?
3. Enlarged NT (≥3.5 mm) in the first trimester – not all chromosome aberrations can be detected by NIPT
4. Microarray and RASopathy‐disorder testing in fetuses with increased nuchal translucency
5. Practice Bulletin No. 162
Cited by 8 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. Selection of prenatal screening with nuchal translucency > 95th centile and below 99th centile: a 4-year observational study with real-world data;Archives of Gynecology and Obstetrics;2024-04-16
2. Associations between genomic aberrations, increased nuchal translucency, and pregnancy outcomes: a comprehensive analysis of 2,272 singleton pregnancies in women under 35;Frontiers in Medicine;2024-04-03
3. Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound;Taiwanese Journal of Obstetrics and Gynecology;2024-03
4. The Role of Thickened Nuchal Translucency on Copy Number Variations and Pregnancy Outcomes in Northeast Coast of Fujian Province, China: A Comparison Between Traditional Karyotyping and Single Nucleotide Polymorphism Array Analysis;2023-08-17
5. When NIPT meets WES, prenatal diagnosticians face the dilemma: genetic etiological analysis of 2,328 cases of NT thickening and follow-up of pregnancy outcomes;Frontiers in Genetics;2023-08-02
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