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Endocrine Manifestations of Von Hippel–Landau Disease

Von Hippel–Lindau (VHL) disease is an autosomal dominant disorder characterized by various endocrine, nonendocrine, benign, and malignant tumors in various organs. VHL tumor suppressor gene, located on short arm of chromosome 3 is responsible for this. Pheochromocytoma (PCC) is one of the important...

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Bibliografski detalji
Izdano u:Indian J Endocrinol Metab
Glavni autori: Pradhan, Roma, George, Nelson, Mandal, Kaushik, Agarwal, Amit, Gupta, Sushil K.
Format: Artigo
Jezik:Inglês
Izdano: Wolters Kluwer - Medknow 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6446673/
https://ncbi.nlm.nih.gov/pubmed/31016171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijem.IJEM_252_18
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