Associated Papers
Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes.
Woodward ER et al.
Journal of Medical Genetics, 2000
Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations.
Duerr EM et al.
The Journal of Clinical Endocrinology and Metabolism, 1999
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