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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...
Uloženo v:
| Vydáno v: | Indian J Endocrinol Metab |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Wolters Kluwer - Medknow
2019
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| Témata: | |
| On-line přístup: | 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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