Orphanet Journal of Rare Diseases (Feb 2022)

Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia

  • Alicia Scocchia,
  • Tiia Kangas-Kontio,
  • Melita Irving,
  • Matti Hero,
  • Inka Saarinen,
  • Liisa Pelttari,
  • Kimberly Gall,
  • Satu Valo,
  • Johanna M. Huusko,
  • Jonna Tallila,
  • Johanna Sistonen,
  • Juha Koskenvuo,
  • Tero-Pekka Alastalo

DOI
https://doi.org/10.1186/s13023-022-02242-8
Journal volume & issue
Vol. 17, no. 1
pp. 1 – 1

Abstract

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