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

Alicia Scocchia1, Tiia Kangas-Kontio2, Melita Irving3

  • 1Blueprint Genetics Inc, Seattle, WA, USA.

Orphanet Journal of Rare Diseases
|February 18, 2022
PubMed
Abstract

No abstract available in PubMed .

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