Cite
HARVARD Citation
Laurie, S. et al. (2022). The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases. Human mutation. 43 (6), pp. 717-733. [Online].
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Laurie, S. et al. (2022). The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases. Human mutation. 43 (6), pp. 717-733. [Online].