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6. Milone, Roberta, Gnazzo, Maria, Stefanutti, Elena, Serafin, Dorella, Novelli, Antonio. 2019. A new missense mutation in DPF2 gene related to Coffin Siris syndrome 7: Description of a mild phenotype expanding DPF2-related clinical spectrum and differential diagnosis among similar syndromes epigenetically determined. In Brain & development, 42, 192-198. doi:10.1016/j.braindev.2019.10.007. https://pubmed.ncbi.nlm.nih.gov/31706665/
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