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Open Access

Correction

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
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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. 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. https://doi.org/10.1371/journal.pone.0201041 pmid:30091983

Citation: Gieldon L, Mackenroth L, Kahlert A-K, Lemke JR, Porrmann J, Schallner J, et al. (2020) Correction: Diagnostic value of partial exome sequencing in developmental disorders. PLoS ONE 15(9): e0239959. https://doi.org/10.1371/journal.pone.0239959

Published: September 24, 2020

Copyright: © 2020 Gieldon et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.