Alhawari, H., Obeidat, Z., Wahbeh, L., Mismar, A., Younis, N., Jafar, H., . . . Alhawari, H. 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. Taylor & Francis Group.
Chicago Style (17th ed.) CitationAlhawari, 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. Taylor & Francis Group.
MLA (9th ed.) CitationAlhawari, 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. Taylor & Francis Group.