Correction to: Genetics in Medicine; https://doi.org/10.1038/s41436-019-0563-5, published online 07 June 2019
In the original version of this Article, several individuals were erroneously acknowledged in the acknowledgements, they have been removed. The Acknowledgement section in the PDF and HTML versions of the Article has now been corrected to the following:
This study was coordinated by the Newborn Hearing Screening Working Group of the National Coordinating Center for the Regional Genetics Networks. In addition to the authors of the manuscript, the working group included the following members who all contributed to conceptualization, critical commentary, and review of the final manuscript: Ahmad Abou Tayoun, PhD, FACMG, Division of Genomic Diagnostics, Children’s Hospital of Philadelphia, Philadelphia, PA; Kathleen Arnos, PhD, Department of Science, Technology and Math, Gallaudet University, Washington, DC; Gail Demmler-Harrison, MD, Department of Pediatrics and Pathology & Immunology, Baylor College of Medicine, Houston, TX; Terese Finitzo, PhD, F-ASHA, FAAA, Oz Systems, Arlington, TX; David Flannery, MD, American College of Medical Genetics and Genomics, Bethesda, MD; Aaron Goldenberg, PhD, MPH, Department of Bioethics, Case Western Reserve University, Cleveland, OH; Cathy Harbison, RN, Missouri Newborn Hearing Screening Program, Missouri Department of Health and Senior Services, Jefferson City, MO; Nannette Nicholson, PhD, CCC-A, Department of Audiology and Speech Pathology, University of Arkansas for Medical Sciences, Little Rock, AR; Teresa Nold, South Dakota Parent Connection, Sioux Falls, SD; Arti Pandya, MD, MBA, Division of Genetics and Metabolism, Department of Pediatrics, University of North Carolina-Chapel Hill, Chapel Hill, NC; Nathaniel Robin, MD, Department of Genetics, University of Alabama at Birmingham School of Health Professionals, Birmingham, AL; Michael Watson, PhD, MS, FACMG, American College of Medical Genetics and Genomics, Bethesda, MD; Karl White, PhD, National Center for Hearing Assessment and Management, Utah State University, Logan, UT; Lindsey Woodard, Arkansas Hands and Voices, Conway, AR. This project was supported by the Health Resources and Services Administration (HRSA) of the US Department of Health and Human Services (HHS) under #U22MC24100 (National Coordinating Center for the Regional Genetic Services Collaboratives) for $100,000. This information or content and conclusions are those of the author and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS, or the US Government. Other funding received: NIDCD R01s DC003544, DC002842, and DC012049 to R.J.S.; NIDCD R01DC015052 to C.C.M.
Author information
Authors and Affiliations
Consortia
Corresponding authors
Additional information
#Full list of working group members is included in Acknowledgements.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. If you remix, transform, or build upon this article or a part thereof, you must distribute your contributions under the same license as the original. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/.
About this article
Cite this article
Shearer, A.E., Shen, J., Amr, S. et al. Correction: A proposal for comprehensive newborn hearing screening to improve identification of deaf and hard-of-hearing children. Genet Med 21, 2845–2846 (2019). https://doi.org/10.1038/s41436-019-0587-x
Published:
Issue Date:
DOI: https://doi.org/10.1038/s41436-019-0587-x