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APA Citation
Watson, C. M., Crinnion, L. A., Tzika, A., Mills, A., Coates, A., Pendlebury, M., Hewitt, S., Harrison, S. M., Daly, C., Roberts, P., Carr, I. M., Sheridan, E. G., & Bonthron, D. T. (n.d.). diagnostic whole genome sequencing and split‐read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome. American journal of medical genetics, 164(10), 2649–2655. http://access.bl.uk/ark:/81055/vdc_100089669296.0x000018