APA (7th ed.) Citation

Alhawari, H., Obeidat, Z., Wahbeh, L., Mismar, A., Younis, N., Jafar, H., . . . Alhawari, H. (2024). Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype. Blood Pressure, 33(1), 1. https://doi.org/10.1080/08037051.2024.2355268

Chicago Style (17th ed.) Citation

Alhawari, Hussein, et al. "Discovering a Novel Genetic Variant in 11 Family Members Who Had Isolated Pheochromocytoma Linked to Von Hippel-Lindau (VHL) Syndrome, Aligning with the Type 2c Phenotype." Blood Pressure 33, no. 1 (2024): 1. https://doi.org/10.1080/08037051.2024.2355268.

MLA (9th ed.) Citation

Alhawari, Hussein, et al. "Discovering a Novel Genetic Variant in 11 Family Members Who Had Isolated Pheochromocytoma Linked to Von Hippel-Lindau (VHL) Syndrome, Aligning with the Type 2c Phenotype." Blood Pressure, vol. 33, no. 1, 2024, p. 1, https://doi.org/10.1080/08037051.2024.2355268.