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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.

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Title: 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.
Authors: Alhawari, Hussein1 (AUTHOR) h.alhawari@ju.edu.jo, Obeidat, Zaina1 (AUTHOR), Wahbeh, Lina1 (AUTHOR), Mismar, Ayman2 (AUTHOR), Younis, Nedal2 (AUTHOR), Jafar, Hanan1 (AUTHOR), Momani, Munther1 (AUTHOR), Alsabatin, Nedal2 (AUTHOR), Awidi, Abdalla1 (AUTHOR), Alhawari, Hussam1 (AUTHOR)
Source: Blood Pressure. Aug2024, Vol. 33 Issue 1, p1-6. 6p.
Database: Academic Search Ultimate
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  Data: 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.
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  Data: <searchLink fieldCode="JN" term="%22Blood+Pressure%22">Blood Pressure</searchLink>. Aug2024, Vol. 33 Issue 1, p1-6. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=182506623
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        Value: 10.1080/08037051.2024.2355268
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              Text: Aug2024
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