AMA
Murawska A, Możdżeń K, Horosin G, et al. Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene. Pediatria Polska - Polish Journal of Paediatrics. 2024;99(4):378-384. doi:10.5114/polp.2024.143885.
APA
Murawska, A., Możdżeń, K., Horosin, G., Pędziwiatr, E., Makowska, J., & Pośpiech, J. et al. (2024). Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene. Pediatria Polska - Polish Journal of Paediatrics, 99(4), 378-384. https://doi.org/10.5114/polp.2024.143885
Chicago
Murawska, Agnieszka, Kamil Możdżeń, Grzegorz Horosin, Edward Pędziwiatr, Joanna Makowska, Jakub Pośpiech, and Konrad Kaleta et al. 2024. "Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene". Pediatria Polska - Polish Journal of Paediatrics 99 (4): 378-384. doi:10.5114/polp.2024.143885.
Harvard
Murawska, A., Możdżeń, K., Horosin, G., Pędziwiatr, E., Makowska, J., Pośpiech, J., Kaleta, K., Drożdż, D., and Zachwieja, K. (2024). Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene. Pediatria Polska - Polish Journal of Paediatrics, 99(4), pp.378-384. https://doi.org/10.5114/polp.2024.143885
MLA
Murawska, Agnieszka et al. "Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene." Pediatria Polska - Polish Journal of Paediatrics, vol. 99, no. 4, 2024, pp. 378-384. doi:10.5114/polp.2024.143885.
Vancouver
Murawska A, Możdżeń K, Horosin G, Pędziwiatr E, Makowska J, Pośpiech J et al. Case report of twins with Bardet-Biedl syndrome exhibiting a rare mutation in the TTC8 gene. Pediatria Polska - Polish Journal of Paediatrics. 2024;99(4):378-384. doi:10.5114/polp.2024.143885.
