Background: Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors arising from chromaffin cells in the adrenal medulla and extra-adrenal ganglia, respectively. The study was aimed t
Values in parentheses indicate percentage of SFP detected/escaped by gene-chip. Table includes SFP data analyzed at estimated 9.5% FDR in CP&LG and 9% FDR in CP&RT dataset. CP = Cypress, LG = LaGrue,
