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Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia
Orphanet Journal of Rare Diseases volume 17, Article number: 59 (2022)
The Original Article was published on 09 October 2021
Correction to: Orphanet J Rare Dis (2021) 16:412 https://doi.org/10.1186/s13023-021-02025-7
Following the publication of the original article [1] the authors noticed an inconsistency between the following sentences:
“Diagnostic yield was significantly higher among fetal samples (58.0%, n = 51/88) than postnatal samples (38.9%, n = 177/455; z = 3.32, p < 0.0009)” in the “Results” section of the “Abstract”
and
“Diagnostic yield was significantly higher among fetal samples (58.0%, n = 51/88) compared to postnatal samples (38.9%, n = 177/455; z = 3.32, p < 0.0001)” in the “Results” section of the main text.
The correct information is the one reported in Figure 2: “Diagnostic yield was significantly higher among fetal samples (59.0%, n = 52/88) than postnatal samples (38.7%, n = 176/455; z = 3.55, p < 0.001)”.
The original article has now been updated with the “Results” section of the “Abstract” and “Results” section of the main text having been corrected as per Figure 2.
Reference
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. https://doi.org/10.1186/s13023-021-02025-7.
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Scocchia, A., Kangas-Kontio, T., Irving, M. et al. Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia. Orphanet J Rare Dis 17, 59 (2022). https://doi.org/10.1186/s13023-022-02242-8
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DOI: https://doi.org/10.1186/s13023-022-02242-8