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. - Alhawari, Hussein; Obeidat, Zaina; Wahbeh, Lina; Mismar, Ayman; Younis, Nedal; Jafar, Hanan; Momani, Munther; Alsabatin, Nedal; Awidi, Abdalla; Alhawari, Hussam (Blood Pressure, 2024)