Anwendung genetischer Untersuchungen in der Pränataldiagnostik
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-662-44369-9_7-2
Reference68 articles.
1. ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis. (2009) Obstet Gynecol 114:1161–1163. https://doi.org/10.1097/AOG.0B013E3181C33CAD
2. Ashoor G, Syngelaki A, Poon LCY et al (2013) Fetal fraction in maternal plasma cell-free DNA at 11–13 weeks’ gestation: relation to maternal and fetal characteristics. Ultrasound Obstet Gynecol 41:26–32. https://doi.org/10.1002/UOG.12331
3. Benn P, Chapman AR (2016) Ethical and practical challenges in providing noninvasive prenatal testing for chromosome abnormalities: an update. Curr Opin Obstet Gynecol 28:119–124. https://doi.org/10.1097/GCO.0000000000000254
4. Best S, Wou K, Vora N et al (2018) Promises, pitfalls and practicalities of prenatal whole exome sequencing. Prenat Diagn 38:10–19. https://doi.org/10.1002/PD.5102
5. Bevilacqua E, Ordóñez E, Hurtado I et al (2018) Screening for sex chromosome aneuploidy by cell-free DNA testing: patient choice and performance. Fetal Diagn Ther 44:98–104. https://doi.org/10.1159/000479507
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