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HARVARD Citation
Conlin, L. et al. (2022). Long‐read sequencing for molecular diagnostics in constitutional genetic disorders. Human mutation. 43 (11), pp. 1531-1544. [Online].
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Conlin, L. et al. (2022). Long‐read sequencing for molecular diagnostics in constitutional genetic disorders. Human mutation. 43 (11), pp. 1531-1544. [Online].