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

Overview of attention for article published in Orphanet Journal of Rare Diseases, February 2022

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RT @dazzle4rare: Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeleta…

19 Feb 2022

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Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia https://t.co/rvMzgPq6vQ

19 Feb 2022

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