Article Versions Notes

Sparago A, Cerrato F, Pignata L, Cammarata-Scalisi F, Garavelli L, Piscopo C, Vancini A, Riccio A. Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C. Genes. 2021; 12(5):706. https://doi.org/10.3390/genes12050706

Sparago, Angela, Flavia Cerrato, Laura Pignata, Francisco Cammarata-Scalisi, Livia Garavelli, Carmelo Piscopo, Alessandra Vancini, and Andrea Riccio. 2021. "Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C" Genes 12, no. 5: 706. https://doi.org/10.3390/genes12050706

Sparago, A., Cerrato, F., Pignata, L., Cammarata-Scalisi, F., Garavelli, L., Piscopo, C., Vancini, A., & Riccio, A. (2021). Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C. Genes, 12(5), 706. https://doi.org/10.3390/genes12050706