1. Analysis of mutations in EPOR, VHL, EPAS1 and EGLN1 genes associated with the familial erythrocytosis ECYT1-4 among JAK2- and CALR-negative patients with the erythrocytosis of unclear etiology
   T. N. Subbotina et al, 2023, Russian journal of hematology and transfusiology CrossRef
2. The Role of VHL in the Development of von Hippel-Lindau Disease and Erythrocytosis
   Petra Hudler et al, 2022, Genes CrossRef
3. Retinal hemangioblastoma in a patient with Von Hippel-Lindau disease: A case report and literature review
   Yikeng Huang et al, 2022, Frontiers in Oncology CrossRef
4. VHL syndrome without clear family history: A rare case report and literature review of Chinese patients
   Yaheng Li et al, 2022, Frontiers in Neurology CrossRef