Cite
MLA Citation
Lipika R. Pal et al.. “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, vol. 41, no. 2, 2020, pp. 347–362. http://access.bl.uk/ark:/81055/vdc_100099420160.0x000031