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Case Reports in Genetics
Volume 2015, Article ID 926545, 7 pages
http://dx.doi.org/10.1155/2015/926545
Case Report

Unexplained False Negative Results in Noninvasive Prenatal Testing: Two Cases Involving Trisomies 13 and 18

1Department of Medical Genetics, Division of Biomedical Genetics, University Medical Centre Utrecht, P.O. Box 85090, Mail Stop KC04.084.2, 3508 AB Utrecht, Netherlands
2Department of Obstetrics and Gynecology, University Medical Centre Utrecht, P.O. Box 85090, Mail Stop KE04.123.1, 3508 AB Utrecht, Netherlands

Received 18 March 2015; Accepted 26 May 2015

Academic Editor: Philip D. Cotter

Copyright © 2015 R. Hochstenbach et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [4 citations]

The following is the list of published articles that have cited the current article.

  • Martin Poot, “To NIPT or Not to NIPT.,” Molecular syndromology, vol. 6, no. 4, pp. 153–5, 2015. View at Publisher · View at Google Scholar
  • Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar, and François Rousseau, “Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues.,” The application of clinical genetics, vol. 9, pp. 15–26, 2016. View at Publisher · View at Google Scholar
  • Yang Cao, Nicole L. Hoppman, Sarah E. Kerr, Christopher A. Sattler, Kristi S. Borowski, Myra J. Wick, W. Edward Highsmith, and Umut Aypar, “False Negative Cell-Free DNA Screening Result in a Newborn with Trisomy 13,” Case Reports in Genetics, vol. 2016, pp. 1–5, 2016. View at Publisher · View at Google Scholar
  • Tanja Schlaikjaer Hartwig, Louise Ambye, Steen Sørensen, and Finn Stener Jørgensen, “Discordant non-invasive prenatal testing (NIPT) - a systematic review,” Prenatal Diagnosis, 2017. View at Publisher · View at Google Scholar