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

被引：0
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作者：
Alicia Scocchia
Tiia Kangas-Kontio
Melita Irving
Matti Hero
Inka Saarinen
Liisa Pelttari
Kimberly Gall
Satu Valo
Johanna M. Huusko
Jonna Tallila
Johanna Sistonen
Juha Koskenvuo
Tero-Pekka Alastalo
机构：
[1] Blueprint Genetics Inc,Department of Clinical Genetics
[2] Blueprint Genetics Oy,New Children’s Hospital, Pediatric Research Center
[3] Guy’s and St. Thomas’ NHS Trust,undefined
[4] Helsinki University Hospital,undefined
来源：
Orphanet Journal of Rare Diseases | / 17卷
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