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APA Citation
Pal, L. R., Kundu, K., Yin, Y., & Moult, J. (2020). matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype‐weighted knowledge in the CAGI SickKids5 clinical genomes challenge. Human mutation, 41(2), 347–362. http://access.bl.uk/ark:/81055/vdc_100099420160.0x000031