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HARVARD Citation
Alankarage, D. et al. (2020). Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human molecular genetics. pp. 1068-1082. [Online].
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Alankarage, D. et al. (2020). Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. Human molecular genetics. pp. 1068-1082. [Online].