Familial pheochromocytoma due to mutant von Hippel Lindau disease gene

被引：10

作者：

Mulvihill, JJ

Ferrell, RE

Carty, SE

Tisherman, SE

Zbar, B

机构：

来源：

ARCHIVES OF INTERNAL MEDICINE | 1997年 / 157卷 / 12期

关键词：

D O I：

10.1001/archinte.157.12.1390

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1390 / 1391

页数：2

共 7 条

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LI, H ;

WEI, MH ;

SCHMIDT, L ;

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LINEHAN, WM ;

LERMAN, M ;

ZBAR, B .

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[2] Genotype-phenotype correlation in vonHippel-Lindau disease: Identification of a mutation associated with VHL type 2A [J].

Chen, F ;

SLife, L ;

Kishida, T ;

Mulvihill, J ;

Tisherman, SE ;

Zbar, B .

JOURNAL OF MEDICAL GENETICS, 1996, 33 (08) :716-717

[3] MOLECULAR-GENETIC DIAGNOSIS OF VON HIPPEL-LINDAU DISEASE IN FAMILIAL PHEOCHROMOCYTOMA [J].

CROSSEY, PA ;

ENG, C ;

GINALSKAMALINOWSKA, M ;

LENNARD, TWJ ;

WHEELER, DC ;

PONDER, BAJ ;

MAHER, ER .

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[4]

TISHERMAN SE, 1993, ARCH INTERN MED, V153, P2550

[5]

TISHERMAN SE, 1962, JAMA-J AM MED ASSOC, V263, P152

[6]

Zbar B, 1996, HUM MUTAT, V8, P348, DOI 10.1002/(SICI)1098-1004(1996)8:4<348::AID-HUMU8>3.0.CO

[7]

2-3

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