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PDFDiagnostics
Review
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
- Correspondence to Dr David Bick, HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA; dbick{at}hudsonalpha.org
Citation
Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
Publication history
- Received February 25, 2019
- Accepted March 19, 2019
- First published April 25, 2019.
Online issue publication
November 27, 2019
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- Previous version (25 April 2019).
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© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.