Article info
PDFDevelopmental defects
Review
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
- Correspondence to Dr Antonio Musio, Istituto di Ricerca Genetica e Biomedica, Pisa 56124, Italy; antonio.musio{at}irgb.cnr.it
Citation
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
Publication history
- Received May 8, 2019
- Revised August 8, 2019
- Accepted October 2, 2019
- First published November 8, 2019.
Online issue publication
April 23, 2020
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© Author(s) (or their employer(s)) 2020. 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/.