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APA Citation
Foreman, J., Brent, S., Perrett, D., Bevan, A. P., Hunt, S. E., Cunningham, F., Hurles, M. E., & Firth, H. V. (2022). dECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research. Human mutation, 43(6), 682–697. http://access.bl.uk/ark:/81055/vdc_100155166167.0x00000f