Published in Surgery Litigation and Law Weekly, November 2nd, 2007
"This is the first report on the combination of a neuroendocrine pancreatic tumor with adrenal pheochromocytoma in a pediatric patient with von Hippel-Lindau (VHL) disease. von Hippel-Lindau disease was confirmed by molecular genetic analysis of peripheral blood lymphocytes, which revealed the mutation VHL c. 695 G> A. The family history showed also VHL disease in the mother who carried...
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