Noninvasive prenatal testing: from aneuploidy to single genes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s00439-019-02061-1.pdf
Reference58 articles.
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2. Ashoor G, Syngelaki A, Poon LC, Rezende JC, Nicolaides KH (2013) Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks’ gestation: relation to maternal and fetal characteristics. Ultrasound Obstet Gynecol 41(1):26–32. https://doi.org/10.1002/uog.12331 (Epub 2012 Dec 4)
3. Bevilacqua E, Gil MM, Nicolaides KH, Ordoñez E, Cirigliano V, Dierickx H, Willems PJ, Jani JC (2015) Performance of screening for aneuploidies by cell-free DNA analysis of maternal blood in twin pregnancies. Ultrasound Obstet Gynecol 45(1):61–66. https://doi.org/10.1002/uog.14690 (Epub 2014 Dec 4)
4. Bianchi DW (2018) Cherchez la femme: maternal incidental findings can explain discordant prenatal cell-free DNA sequencing results. Genet Med. 20(9):910–917. https://doi.org/10.1038/gim.2017.219 (Epub 2017 Dec 7. Review)
5. Bianchi DW, Chiu RWK (2018) Sequencing of circulating cell-free DNA during pregnancy. N Engl J Med 379(5):464–473. https://doi.org/10.1056/nejmra1705345 (Review. PubMed PMID: 30067923)
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