Whole‐exome sequencing and immunohistochemistry findings in von Hippel–Lindau disease

BACKGROUND: von Hippel–Lindau (VHL) disease has a hereditary, autosomal dominant pattern, and multiple tumors can develop in multiple organs of a single patient. However, the exact mechanisms of tumorigenesis are unclear, and further studies are needed to clarify whether the same signaling pathways...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Xiaopeng, Gao, Lu, Hong, Xiafei, Guo, Dan, Di, Wenyu, Wang, Xiaoman, Xu, Zhiqin, Xing, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732316/
https://www.ncbi.nlm.nih.gov/pubmed/31317677
http://dx.doi.org/10.1002/mgg3.880

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732316/
https://www.ncbi.nlm.nih.gov/pubmed/31317677
http://dx.doi.org/10.1002/mgg3.880

Ejemplares similares