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Original Article
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

Authors

  1. Correspondence to Dr Maria Clara Bonaglia, Cytogenetics Laboratory, Scientific Institute IRCCS Eugenio Medea, Bosisio Parini 23842, Italy; clara.bonaglia{at}bp.lnf.it
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Citation

Kurtas N, Arrigoni F, Errichiello E, et al
Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

Publication history

  • Received 23 October 2017
  • Revised 21 December 2017
  • Accepted 8 January 2018
  • Published online 29 January 2018.

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