Priolo, M.;                     Radio, F.C.;                     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, 1009.
    https://doi.org/10.3390/genes12071009
    AMA Style
    
                                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
    
    Chicago/Turabian Style
    
                                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
    
    APA Style
    
                                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