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Published Erratum
. 2022 Feb 17;17(1):59.
doi: 10.1186/s13023-022-02242-8.

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

Alicia Scocchia  1 , Tiia Kangas-Kontio  2 , Melita Irving  3 , Matti Hero  2   4 , Inka Saarinen  2 , Liisa Pelttari  2 , Kimberly Gall  1 , Satu Valo  2 , Johanna M Huusko  2 , Jonna Tallila  2 , Johanna Sistonen  2 , Juha Koskenvuo  2 , Tero-Pekka Alastalo  5
Affiliations
Published Erratum

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

Alicia Scocchia et al. Orphanet J Rare Dis. .
No abstract available

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References

    1. Scocchia et al., Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia, Orphanet J Rare Dis (2021) 16:412. 10.1186/s13023-021-02025-7. - PMC - PubMed

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