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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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Detalhes bibliográficos
Publicado no:Indian J Endocrinol Metab
Main Authors: Pradhan, Roma, George, Nelson, Mandal, Kaushik, Agarwal, Amit, Gupta, Sushil K.
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer - Medknow 2019
Assuntos:
Acesso em linha: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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