Case Reports in Genetics
Volume 2019 (2019), Article ID 4361630, 1 page
https://doi.org/10.1155/2019/4361630

Corrigendum

Corrigendum to “Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features”

Jacquelyn D. Riley,¹ Catherine M. Stefaniuk,1,2 Francine Erenberg,³ Angelika L. Erwin,⁴ Lauren Palange,⁴ and Caroline Astbury¹

¹Molecular Pathology Section, Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA
²Department of Pathology and Laboratory Medicine, University of Cincinnati Health, Cincinnati, OH, USA
³Pediatric Cardiology, Pediatric Institute, Cleveland Clinic, Cleveland, OH, USA
⁴Center for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH, USA

Correspondence should be addressed to Caroline Astbury; astburc@ccf.org

Received 18 September 2019; Accepted 1 October 2019; Published 24 November 2019

Copyright © 2019 Jacquelyn D. Riley et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

In the article titled “Chromosome 3p Inverted Duplication with Terminal Deletion: Second Postnatal Case Report with Additional Clinical Features” [1], the first and third affiliations were incomplete. The corrected authors’ list and affiliations are shown above.

References

J. D. Riley, C. M. Stefaniuk, F. Erenberg, A. L. Erwin, L. Palange, and C. Astbury, “Chromosome 3p inverted duplication with terminal deletion: second postnatal case report with additional clinical features,” Case Reports in Genetics, vol. 2019, Article ID 5384295, 7 pages, 2019.