Article Versions Notes

Mencarelli A, Prontera P, Mencarelli A, Rogaia D, Stangoni G, Cecconi M, Esposito S. Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New “c.[5867T>A]+[=]”; “p.[Leu1956Gln]+[=]” NSD1 Missense Mutation and Complex Skin Hamartoma. International Journal of Molecular Sciences. 2018; 19(10):3189. https://doi.org/10.3390/ijms19103189

Mencarelli, Annalisa, Paolo Prontera, Amedea Mencarelli, Daniela Rogaia, Gabriela Stangoni, Massimiliano Cecconi, and Susanna Esposito. 2018. "Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New “c.[5867T>A]+[=]”; “p.[Leu1956Gln]+[=]” NSD1 Missense Mutation and Complex Skin Hamartoma" International Journal of Molecular Sciences 19, no. 10: 3189. https://doi.org/10.3390/ijms19103189

Mencarelli, A., Prontera, P., Mencarelli, A., Rogaia, D., Stangoni, G., Cecconi, M., & Esposito, S. (2018). Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New “c.[5867T>A]+[=]”; “p.[Leu1956Gln]+[=]” NSD1 Missense Mutation and Complex Skin Hamartoma. International Journal of Molecular Sciences, 19(10), 3189. https://doi.org/10.3390/ijms19103189