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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: May 28, 2023. (Total: 217323Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Pheochromocytoma and MEN1[original query]
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.
The Journal of clinical endocrinology and metabolism 2014 Jul 99 (7): E1352-60.
Welander Jenny, Andreasson Adam, Juhlin C Christofer, Wiseman Roger W, Bäckdahl Martin, Höög Anders, Larsson Catharina, Gimm Oliver, Söderkvist Pet
Pancreatic Neuroendocrine Neoplasm Associated with a Familial MAX Deletion.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2020 6 52 (11): 784-787.
Petignot Sandrine, Daly Adrian F, Castermans Emilie, Korpershoek Esther, Scagnol Irène, Beckers Pablo, Dideberg Vinciane, Rohmer Vincent, Bours Vincent, Beckers Albe
The recurrent p.(Pro540Ser) MEN1 genetic variant should be considered nonpathogenic: A case report.
American journal of medical genetics. Part A 2021 7 185 (12): 3872-3876.
Villabona Carles, Oriola Josep, Serrano Teresa, Guerrero-Pérez Fernando, Valdés Nuria, Chiara Mariló, Robledo Merced
[MEN for multiple endocrin neoplasms: When evokate MEN? Update 2022].
La Revue de medecine interne 2022 10 44 (1): 12-18.
Duval M, Haissaguerre
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