Article Versions Notes

Migliore C, Vendramin A, McKee S, Prontera P, Faravelli F, Sachdev R, Dias P, Mascaro M, Licastro D, Meroni G. SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome. Genes. 2022; 13(2):252. https://doi.org/10.3390/genes13020252

Migliore, Chiara, Anna Vendramin, Shane McKee, Paolo Prontera, Francesca Faravelli, Rani Sachdev, Patricia Dias, Martina Mascaro, Danilo Licastro, and Germana Meroni. 2022. "SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome" Genes 13, no. 2: 252. https://doi.org/10.3390/genes13020252

Migliore, C., Vendramin, A., McKee, S., Prontera, P., Faravelli, F., Sachdev, R., Dias, P., Mascaro, M., Licastro, D., & Meroni, G. (2022). SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome. Genes, 13(2), 252. https://doi.org/10.3390/genes13020252