Associated Papers
VHL syndrome without clear family history: A rare case report and literature review of Chinese patients.
Li Y et al.
Frontiers in Neurology, 2022
The importance of genetic study and long-term management in patients with bilateral pheochromocytomas.
Bellarbi DE et al.
Archive of Clinical Cases, 2019
A Single-Nucleotide Polymorphism of miR-196a2T>C rs11614913 Is Associated with Hepatocellular Carcinoma in the Chinese Population.
Li J et al.
Genetic Testing and Molecular Biomarkers, 2016
A single nucleotide polymorphism in the promoter region of let-7 family is associated with lung cancer risk in Chinese.
Shen LQ et al.
Genetics and Molecular Research : Gmr, 2015
A c.464T>a mutation in VHL gene in a Chinese family with VHL syndrome.
Lu Y et al.
Journal of Neuro-oncology, 2013
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