Associated Papers
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An integrated computational approach can classify VHL missense mutations according to risk of clear cell renal carcinoma.
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Human Molecular Genetics, 2014
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Supplement: supp_ddu321_ddu321supp.docx
Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
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European Journal of Endocrinology, 2009
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