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APA Citation
Paciorkowski, A. R., Keppler‐Noreuil, K., Robinson, L., Sullivan, C., Sajan, S., Christian, S. L., Bukshpun, P., Gabriel, S. B., Gleeson, J. G., Sherr, E. H., & Dobyns, W. B. (n.d.). deletion 16p13.11 uncovers NDE1 mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption. American journal of medical genetics, 161(7), 1523–1530. http://access.bl.uk/ark:/81055/vdc_100024733537.0x000061