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Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia
| Autores principales: | , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851804/ https://www.ncbi.nlm.nih.gov/pubmed/35177119 http://dx.doi.org/10.1186/s13023-022-02242-8 |
| _version_ | 1784652899999023104 |
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| author | 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 |
| author_facet | 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 |
| author_sort | Scocchia, Alicia |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-8851804 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-88518042022-02-22 Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia 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 Orphanet J Rare Dis Correction BioMed Central 2022-02-17 /pmc/articles/PMC8851804/ /pubmed/35177119 http://dx.doi.org/10.1186/s13023-022-02242-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
| spellingShingle | Correction 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 Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title | Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title_full | Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title_fullStr | Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title_full_unstemmed | Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title_short | Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| title_sort | correction to: diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851804/ https://www.ncbi.nlm.nih.gov/pubmed/35177119 http://dx.doi.org/10.1186/s13023-022-02242-8 |
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