Skip to main content
PLOS One logoLink to PLOS One
. 2020 Sep 24;15(9):e0239959. doi: 10.1371/journal.pone.0239959

Correction: Diagnostic value of partial exome sequencing in developmental disorders

Laura Gieldon, Luisa Mackenroth, Anne-Karin Kahlert, Johannes R Lemke, Joseph Porrmann, Jens Schallner, Maja von der Hagen, Susanne Markus, Sabine Weidensee, Barbara Novotna, Charlotte Soerensen, Barbara Klink, Johannes Wagner, Andreas Tzschach, Arne Jahn, Franziska Kuhlee, Karl Hackmann, Evelin Schrock, Nataliya Di Donato, Andreas Rump
PMCID: PMC7514079  PMID: 32970766

Notice of republication

An incorrect version of Fig 2 was published in error. This article was republished on September 4, 2020, to correct for this error. Please download this article again to view the correct version.

Reference

  • 1.Gieldon L, Mackenroth L, Kahlert A-K, Lemke JR, Porrmann J, Schallner J, et al. (2018) Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE 13(8): e0201041 10.1371/journal.pone.0201041 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES