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Passaretti F, Pignata L, Vitiello G, Alesi V, D’Elia G, Cecere F, Acquaviva F, De Brasi D, Novelli A, Riccio A, et al. Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum. Genes. 2022; 13(10):1875. https://doi.org/10.3390/genes13101875

Passaretti, Francesco, Laura Pignata, Giuseppina Vitiello, Viola Alesi, Gemma D’Elia, Francesco Cecere, Fabio Acquaviva, Daniele De Brasi, Antonio Novelli, Andrea Riccio, and et al. 2022. "Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum" Genes 13, no. 10: 1875. https://doi.org/10.3390/genes13101875

Passaretti, F., Pignata, L., Vitiello, G., Alesi, V., D’Elia, G., Cecere, F., Acquaviva, F., De Brasi, D., Novelli, A., Riccio, A., Iolascon, A., & Cerrato, F. (2022). Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum. Genes, 13(10), 1875. https://doi.org/10.3390/genes13101875