Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice

Genet Med. 2020 Aug;22(8):1426. doi: 10.1038/s41436-020-0870-x.

Neeta L Vora¹, Kelly Gilmore², Alicia Brandt³, Chelsea Gustafson³, Natasha Strande^{3

4}, Lori Ramkissoon^{3

4}, Emily Hardisty², Ann Katherine M Foreman³, Kirk Wilhelmsen⁵, Phillips Owen⁶, Karen E Weck^{3

4}, Jonathan S Berg³, Cynthia M Powell^{3

7}, Bradford C Powell³

¹ Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. neeta_vora@med.unc.edu.
² Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
³ Department of Genetics, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
⁴ Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
⁵ Departments of Genetics and Neurology, Renaissance Computing Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
⁶ Renaissance Computing Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
⁷ Department of Pediatrics, Division of Genetics and Metabolism, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.