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Priolo M, Radio FC, Pizzi S, Pintomalli L, Pantaleoni F, Mancini C, Cordeddu V, Africa E, Mammì C, Dallapiccola B, et al. Co-Occurring Heterozygous CNOT3 and SMAD6 Truncating Variants: Unusual Presentation and Refinement of the IDDSADF Phenotype. Genes. 2021; 12(7):1009. https://doi.org/10.3390/genes12071009

Priolo, Manuela, Francesca Clementina Radio, Simone Pizzi, Letizia Pintomalli, Francesca Pantaleoni, Cecilia Mancini, Viviana Cordeddu, Emilio Africa, Corrado Mammì, Bruno Dallapiccola, and et al. 2021. "Co-Occurring Heterozygous CNOT3 and SMAD6 Truncating Variants: Unusual Presentation and Refinement of the IDDSADF Phenotype" Genes 12, no. 7: 1009. https://doi.org/10.3390/genes12071009

Priolo, M., Radio, F. C., Pizzi, S., Pintomalli, L., Pantaleoni, F., Mancini, C., Cordeddu, V., Africa, E., Mammì, C., Dallapiccola, B., & Tartaglia, M. (2021). Co-Occurring Heterozygous CNOT3 and SMAD6 Truncating Variants: Unusual Presentation and Refinement of the IDDSADF Phenotype. Genes, 12(7), 1009. https://doi.org/10.3390/genes12071009