Article Versions Notes

Campobasso G, Mercuri L, De Razza F, Cosentino A, Mele M, Monittola A, Congedo C, Calò MC, Scalcione C, D’Amuri A, et al. Investigating the Role of B9D1 in Meckel–Gruber Syndrome: A Case Report and Comprehensive Literature Review. Genes. 2025; 16(6):643. https://doi.org/10.3390/genes16060643

Campobasso, Gianluca, Ludovica Mercuri, Francesca De Razza, Antonella Cosentino, Marta Mele, Antonella Monittola, Carmen Congedo, Maria Chiara Calò, Caterina Scalcione, Alessandro D’Amuri, and et al. 2025. "Investigating the Role of B9D1 in Meckel–Gruber Syndrome: A Case Report and Comprehensive Literature Review" Genes 16, no. 6: 643. https://doi.org/10.3390/genes16060643

Campobasso, G., Mercuri, L., De Razza, F., Cosentino, A., Mele, M., Monittola, A., Congedo, C., Calò, M. C., Scalcione, C., D’Amuri, A., Mauro, S., & Lattante, S. (2025). Investigating the Role of B9D1 in Meckel–Gruber Syndrome: A Case Report and Comprehensive Literature Review. Genes, 16(6), 643. https://doi.org/10.3390/genes16060643