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Original Article

Pheochromocytoma Associated with Von Hippel-lindau' Disease in a Family

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Pages 259-263 | Received 09 Jan 1970, Published online: 09 Jul 2009

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Joseph H. Chang, Christoph W. Spraul, Michael L. Lynn, Arlene Drack & Hans E. Grossniklaus. (1998) The two-stage mutation model in retinal hemangioblastoma. Ophthalmic Genetics 19:3, pages 123-130.
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Articles from other publishers (5)

F. Resche, J. P. Moisan, J. Mantoura, A. De Kersaint-Gilly, M. J. Andre, I. Perrin-Resche, D. Menegalli-Boggelli, Y. Lajat & S. Richard. 1993. Advances and Technical Standards in Neurosurgery. Advances and Technical Standards in Neurosurgery 197 304 .
Ruben Saranga, Haim Matzkin, Joseph Papo & Zvi Braf. (1989) Von hippel-lindau syndrome with unusual presentations in two brothers. Urology 34:5, pages 301-304.
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Paul Hardwig & Dennis M. Robertson. (1984) von Hippel-Lindau Disease. Ophthalmology 91:3, pages 263-270.
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Joseph J. Kaufman & Stanley Franklin. (1979) Familial Pheochromocytoma: A Report of 2 Cases in a Kindred. Journal of Urology 121:6, pages 801-804.
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R Jeffreys. (1975) Pathological and haematological aspects of posterior fossa haemangioblastomata.. Journal of Neurology, Neurosurgery & Psychiatry 38:2, pages 112-119.
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