Article info
PDFGenome-wide studies
Original Article
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)
- Correspondence to Dr Maria Clara Bonaglia, Cytogenetics Laboratory, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini 23842, Italy; clara.bonaglia{at}bp.lnf.it
Citation
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)
Publication history
- Received October 23, 2017
- Revised December 21, 2017
- Accepted January 8, 2018
- First published January 29, 2018.
Online issue publication
March 22, 2018
Article Versions
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/