Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene

Journal of Clinical Endocrinology and Metabolism

Volumn 81, Issue 1, 1996, Pages 147-149

  Gross, David J ^a   Avishai, Naaman ^a   Meiner, Vardiella ^a   Filon, Dvora ^a   Zbar, Berton ^b   Abeliovich, Dvorah ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADRENAL TUMOR; ADULT; ARTICLE; CHEMODECTOMA; CHILD; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; HEMANGIOBLASTOMA; HUMAN; MALE; NUCLEIC ACID BASE SUBSTITUTION; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; VON HIPPEL LINDAU DISEASE;

ADRENAL GLAND NEOPLASMS; BASE SEQUENCE; CODON; HIPPEL-LINDAU DISEASE; HUMANS; MOLECULAR SEQUENCE DATA; PHEOCHROMOCYTOMA; POINT MUTATION;

EID: 0030064811     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.81.1.147     Document Type: Article

References (16)

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