Prenatal tests for chromosomal abnormalities detection (PTCAD): pregnant women’s knowledge in an Italian Population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynaecology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00404-020-05846-2.pdf
Reference15 articles.
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2. Santorum M, Wright D, Syngelaki A, Karagioti N, Nicolaides KH (2017) Accuracy of first-trimester combined test in screening for trisomies 21, 18 and 13. Ultrasound Obstet Gynecol 49(6):714–720. https://doi.org/10.1002/uog.17283
3. Wulff CB, Gerds TA, Rode L, Ekelund CK, Petersen OB, Tabor A; Danish Foetal Medicine Study Group. Risk of foetal loss associated with invasive testing following combined first-trimester screening for Down syndrome: a national cohort of 147,987 singleton pregnancies. Ultrasound Obstet Gynecol. 2016;47(1):38–44. https://doi.org/10.1002/uog.15820.
4. Mackie FL, Hemming K, Allen S, Morris RK, Kilby MD (2017) The accuracy of cell-free foetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis. BJOG 124(1):32–46. https://doi.org/10.1111/1471-0528.14050
5. Gil MM, Accurti V, Santacruz B, Plana MN, Nicolaides KH. Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis. Ultrasound Obstet Gynecol 2017; 50(3):302–314. https://doi.org/10.1002/uog.17484
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