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APA Citation
Klintman, J., Barmpouti, K., Knight, S. J. L., Robbe, P., Dreau, H., Clifford, R., Ridout, K., Burns, A., Timbs, A., Bruce, D., Antoniou, P., Sosinsky, A., Becq, J., Bentley, D., Hillmen, P., Taylor, J. C., Caulfield, M., & Schuh, A. H. (2018). clinical‐grade validation of whole genome sequencing reveals robust detection of low‐frequency variants and copy number alterations in CLL. British journal of haematology, 182, 412–417. http://access.bl.uk/ark:/81055/vdc_100066550222.0x000060