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Childhood cerebellar hemangioblastoma does not predict germline or somatic mutations in the von Hippel-Lindau tumor suppressor gene

โœ Scribed by Paul Graham Fisher; Art Tontiplaphol; Eric M. Pearlman; Patricia K. Duffner; Douglas J. Hyder; Catherine A. Stolle; Alexander O. Vortmeyer; Zhengping Zhuang

Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
203 KB
Volume
51
Category
Article
ISSN
0364-5134

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โœ Catherine Stolle; Gladys Glenn; Berton Zbar; Jeffrey S. Humphrey; Peter Choyke; ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 201 KB ๐Ÿ‘ 2 views

Communicated by Victor A. McKusick von Hippel-Lindau disease (VHL) is an inherited neoplastic disorder characterized by the development of tumors in the eyes, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis. The VHL tumor suppressor gene was identified in 1993. Initial