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HARVARD Citation
Foreman, J. et al. (2022). DECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research. Human mutation. 43 (6), pp. 682-697. [Online].
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Foreman, J. et al. (2022). DECIPHER: Supporting the interpretation and sharing of rare disease phenotype‐linked variant data to advance diagnosis and research. Human mutation. 43 (6), pp. 682-697. [Online].