Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,General Medicine
Link
http://link.springer.com/article/10.1007/s00404-017-4459-9/fulltext.html
Reference55 articles.
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3. Nicolaides KH, Azar G, Byrne D et al (1992) Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy. BMJ 304:867–869
4. Cuckle H, Maymon R (2016) Development of prenatal screening—a historical overview. Semin Perinatol 40:12–22. doi: 10.1053/j.semperi.2015.11.003
5. Spencer K, Souter V, Tul N et al (1999) A screening program for trisomy 21 at 10–14 weeks using fetal nuchal translucency, maternal serum free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Ultrasound Obstet Gynecol 13:231–237. doi: 10.1046/j.1469-0705.1999.13040231.x
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