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HARVARD Citation
Alharatani, R. et al. (2020). Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. Human molecular genetics. pp. 1900-1921. [Online].
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Alharatani, R. et al. (2020). Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome. Human molecular genetics. pp. 1900-1921. [Online].