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1 VHL gene in the four affected siblings with pancreatic islet cell tumors.
2 s after initial screening, she developed two pancreatic islet cell tumors and a premalignant renal cy
3 e reviews the current clinical management of pancreatic islet cell tumors and describes the molecular
4 e endocrine pancreas, commonly referenced as pancreatic islet cell tumors, are rare, often well diffe
5 ly history that describes the development of pancreatic islet cell tumors in four of five female sibl
6 rmore, we conclude that the preponderance of pancreatic islet cell tumors in this family cannot be ex
7 cts of RCA I on blood vessels of spontaneous pancreatic islet-cell tumors in RIP-Tag2 transgenic mice
8 ma are common lesions; pheochromocytomas and pancreatic islet cell tumors occur less frequently but a
11 e molecular events underlying the biology of pancreatic islet cell tumors will aid the development of
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