Cite
A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2.
MLA
Patricia Migliavacca, Michele, et al. “A Brazilian Case of IFAP Syndrome with Severe Congenital Ichthyosis and Limb Malformations Caused by a Rare Variant in MBTPS2.” Revista Paulista de Pediatria, vol. 41, Jan. 2023, pp. 1–5. EBSCOhost, https://doi.org/10.1590/1984-0462/2023/41/2022057.
APA
Patricia Migliavacca, M., Ambrosio Fock, R., Almeida, N., Cavalcanti, T., Villela, D., Alvarez Perez, A. B., Valle, D., Wohler, E., Lygia de Macena Sobreira, N., & Raskin, S. (2023). A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2. Revista Paulista de Pediatria, 41, 1–5. https://doi.org/10.1590/1984-0462/2023/41/2022057
Chicago
Patricia Migliavacca, Michele, Rodrigo Ambrosio Fock, Nadia Almeida, Thereza Cavalcanti, Darine Villela, Ana Beatriz Alvarez Perez, David Valle, Elizabeth Wohler, Nara Lygia de Macena Sobreira, and Salmo Raskin. 2023. “A Brazilian Case of IFAP Syndrome with Severe Congenital Ichthyosis and Limb Malformations Caused by a Rare Variant in MBTPS2.” Revista Paulista de Pediatria 41 (January): 1–5. doi:10.1590/1984-0462/2023/41/2022057.