Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus-Reference-Cited by-同舟云学术

Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus

Published:1991-06 Issue:2 Volume:87 Page:207-210
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Glenn Gladys M.,Daniel Lambert N.,Choyke Peter,Linehan W. Marston,Oldfield Edward,Gorin Michael B.,Hosoe Shigeto,Latif Farida,Weiss Gary,Walther McClellan,Lerman Michael I.,Zbar Berton

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00204184.pdf

Reference24 articles.

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2. Choyke PL, Filling-Katz MR, Shawker TH, Gorin MB, Travis WD, Chang R, Scizinger B, Linehan WM (1990) Radiologic screening for visceral manifestations of von Hippel-Lindau disease. Genitourin Radiol 174:815?820

3. Filling-Katz MR, Choyke PL, Patronas NJ, Gorin M, Oldfield EH, Barba D, Chang R, Doppmann JL, Scizinger B (1989) Radiologic screening of von Hippel-Lindau disease: the role of MRI in the central nervous system. J Comput Tomogr 13:743?755

4. Glenn GM, Choyke P, Zbar B, Linehan WM (1990) Von Hippel-Lindau disease: clinical review and molecular genetics. Probl Urol 4:312?330

5. Glushein AS, Mansuy MM, Littman DS (1953) Pheochromocytoma: its relationship to neurocutaneous syndromes. Am J Med 14:318?327

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