Cite
HARVARD Citation
Riggs, E. et al. (2018). Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Human mutation. 39 (11), pp. 1650-1659. [Online].
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Riggs, E. et al. (2018). Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar. Human mutation. 39 (11), pp. 1650-1659. [Online].