Cite
HARVARD Citation
Kurtas, N. et al. (2018). Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). Journal of medical genetics. 55 (4), pp. 269-277. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Kurtas, N. et al. (2018). Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). Journal of medical genetics. 55 (4), pp. 269-277. [Online].