Pheochromocytoma in von Hippel-Lindau Disease: Clinical Presentation and Mutation Analysis in a Large, Multigenerational Kindred1-Reference-Cited by-同舟云学术

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Pheochromocytoma in von Hippel-Lindau Disease: Clinical Presentation and Mutation Analysis in a Large, Multigenerational Kindred1

Published:1998-01-01 Issue:1 Volume:83 Page:117-120
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Atuk Nuzhet O.¹,Stolle Catherine¹,Owen John A.¹,Carpenter Johnson T.¹,Vance Mary Lee¹

Affiliation:

1. Nephrology and Endocrinology and Metabolism Divisions, Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908; and Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/83/1/117/9228533/jcem0117.pdf

Reference15 articles.

1. Lindau’s Disease, review of the literature, and study of a large kindred.;Melmon;Am J Med,1964

2. Clinical features and natural history of von Hippel-Lindau Disease.;Maher;Q J Med,1990

3. Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3.;Hosoe;Genomics,1990

4. Identification of the von Hippel-Lindau disease tumor suppressor gene.;Latif;Science,1993

5. Identification of intragenic mutations in von Hippel-Lindau disease tumor suppressor gene and correlation with disease phenotype.;Crossey;Hum Mol Genet,1994

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