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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2015 Oct 15;23(11):1592. doi: 10.1038/ejhg.2015.109

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall, Lidewij Henneman, Heidi C Howard, Anneke Lucassen, Kelly Ormond, Borut Peterlin, Dragica Radojkovic, Wolf Rogowski, Maria Soller, Aad Tibben, Lisbeth Tranebjærg, Carla G van El, Martina C Cornel, on behalf of the European Society of Human Genetics (ESHG) and the American Society of Human Genetics (ASHG)
PMCID: PMC4613480  PMID: 26468681

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.


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