Molecular diagnosis of von Hippel-Lindau disease in a kindred with a predominance of familial phaeochromocytoma

Clinical Endocrinology

Volumn 46, Issue 3, 1997, Pages 359-363

  Garcia, Arnald ^a   Matias Guiu, Xavier ^a,b   Cabezas, Rosa ^a   Chico, Ana ^a   Prat, Jaime ^a   Baiget, Montserrat ^a   De Leiva, Alberto ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DNA DETERMINATION; FAMILIAL DISEASE; FEMALE; GERM CELL; HUMAN; HUMAN TISSUE; MALE; PHEOCHROMOCYTOMA; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; VON HIPPEL LINDAU DISEASE;

EID: 0030896614     PISSN: 03000664     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2265.1997.00149.x     Document Type: Article

References (12)

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