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

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Bibliographic Details
Published in:Orphanet journal of rare diseases 2022-02, Vol.17 (1), p.59-59, Article 59
Main Authors: Scocchia, Alicia, Kangas-Kontio, Tiia, Irving, Melita, Hero, Matti, Saarinen, Inka, Pelttari, Liisa, Gall, Kimberly, Valo, Satu, Huusko, Johanna M, Tallila, Jonna, Sistonen, Johanna, Koskenvuo, Juha, Alastalo, Tero-Pekka
Format: Article
Language:English
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ISSN:1750-1172
1750-1172
DOI:10.1186/s13023-022-02242-8