Correction to: European Journal of Human Genetics advance online publication, 18 March 2015; doi:10.1038/ejhg.2015.57
An error was made when presenting results of the CARE study by Bianchi et al.
The sentence: ‘They found a sensitivity of 100% (for all three trisomies) (95% confidence interval (CI): 99.8–100), at a specificity of 99.7 and 99.8% for trisomies 21 and 18, respectively’ should have read: ‘While detecting all eight cases of the three trisomies, this study found a specificity of 99.7 for trisomy 21 (95% CI: 99.3–99.9) and 99.8 for trisomy 18 (95% CI: 99.6–100).
The authors would like to apologise for their error.
The online version of the original article can be found at 10.1038/ejhg.2015.57
About this article
Cite this article
Dondorp, W., de Wert, G., Bombard, Y. et al. Erratum: Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Eur J Hum Genet 23, 1592 (2015). https://doi.org/10.1038/ejhg.2015.109
Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype
Prenatal Diagnosis (2019)
Endocrine Reviews (2019)
Critical Reviews in Clinical Laboratory Sciences (2019)
The Prevalence of Y-chromosome Microdeletions in Oligozoospermic Men: A Systematic Review and Meta-analysis of European and North American Studies
European Urology (2019)
Clinical Chemistry (2019)