Campobasso, G.; Mercuri, L.; De Razza, F.; Cosentino, A.; Mele, M.; Monittola, A.; Congedo, C.; Calò, M.C.; 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, 643.
https://doi.org/10.3390/genes16060643
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
