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PDFDevelopmental defects
Original research
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
- Correspondence to Professor Judith Melki, Institut National de la Santé et de la Recherche Médicale (Inserm), UMR-1195, INSERM, Paris, Île-de-France 94276, France; judith.melki{at}inserm.fr
Citation
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita
Publication history
- Received November 16, 2020
- Revised February 23, 2021
- Accepted March 14, 2021
- First published April 5, 2021.
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© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/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/.