Cite
HARVARD Citation
Pais, L. et al. (2022). Seqr: A web‐based analysis and collaboration tool for rare disease genomics. Human mutation. 43 (6), pp. 698-707. [Online].
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Pais, L. et al. (2022). Seqr: A web‐based analysis and collaboration tool for rare disease genomics. Human mutation. 43 (6), pp. 698-707. [Online].