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HARVARD Citation
Alesi, V. et al. (2019). A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome. American journal of medical genetics. 179 (8), pp. 1615-1621. [Online].
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Alesi, V. et al. (2019). A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome. American journal of medical genetics. 179 (8), pp. 1615-1621. [Online].