Screening for Chromosomal Defects by Fetal Nuchal Translucency at 11 to 14 Weeks
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Obstetrics and Gynaecology
Reference66 articles.
1. Absence of nasal bone in fetuses with trisomy 21 at 11–14 weeks of gestation: an observational study
2. Using fetal nuchal translucency to screen for major congenital cardiac defects at 10-14 weeks of gestation: population based cohort study
3. Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation
4. Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester
5. Increased nuchal translucency thickness at l0-14 weeks of gestation as a predictor of severe twin-to-twin transfusion syndrome
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