Correction to: European Journal of Human Genetics (2016) 24, 2–5; doi:10.1038/ejhg.2015.226; published online 28 October 2015
Following the publication of this article, the authors wish to append a Supplementary file. This information can be found on European Journal of Human Genetics website http://www.nature.com/ejhg.
Additional information
The online version of the original article can be found at 10.1038/ejhg.2015.226
Supplementary information
Rights and permissions
About this article
Cite this article
Matthijs, G., Souche, E., Alders, M. et al. Erratum: Guidelines for diagnostic next-generation sequencing. Eur J Hum Genet 24, 1515 (2016). https://doi.org/10.1038/ejhg.2016.63
Published:
Issue Date:
DOI: https://doi.org/10.1038/ejhg.2016.63
This article is cited by
-
Multi-omics approaches for precision obesity management
Wiener klinische Wochenschrift (2023)
-
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing
Genome Medicine (2022)
-
Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss
BMC Medical Genetics (2019)
-
Points to consider for laboratories reporting results from diagnostic genomic sequencing
European Journal of Human Genetics (2018)
-
A phenotype centric benchmark of variant prioritisation tools
npj Genomic Medicine (2018)
