Intra-Familial Phenotypic Heterogeneity and Telomere Abnormality in von Hippel- Lindau Disease: Implications for Personalized Surveillance Plan and Pathogenesis of VHL-Associated Tumors

von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome with poor survival. The current recommendations have proposed uniform surveillance strategies for all patients, neglecting the obvious phenotypic varieties. In this study, we aim to confirm the phenotypic heterogeneity in VHL disease an...

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Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: Wang, Jiangyi, Peng, Xiang, Chen, Cen, Ning, Xianghui, Peng, Shuanghe, Li, Teng, Liu, Shengjie, Hong, Baoan, Zhou, Jingcheng, Ma, Kaifang, Cai, Lin, Gong, Kan
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2019
Matèries:
Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6491623/
https://ncbi.nlm.nih.gov/pubmed/31068970
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00358
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