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Volumn 21, Issue 3, 2002, Pages 479-482

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma

(8) Koch, Christian A a Huang, Steve C b Zhuang, Zhengping b Stolle, Catherine c Azumi, Norio d Chrousos, George P a Vortmeyer, Alexander O b,d Pacak, Karel a,d

a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT (United States)

b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE (United States)

c UNIVERSITY OF PENNSYLVANIA (United States)

d GEORGETOWN UNIVERSITY (United States)

Author keywords

Deletion; MEN 2; Pheochromocytoma; RET; VHL

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; ENDOCRINE TUMOR; FAMILY HISTORY; FEMALE; GENE DELETION; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PHEOCHROMOCYTOMA; POINT MUTATION; PRIORITY JOURNAL; SIPPLE SYNDROME; VON HIPPEL LINDAU DISEASE;

ADULT; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; EXONS; FEMALE; GENE DELETION; HUMANS; LIGASES; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A; PHEOCHROMOCYTOMA; POINT MUTATION; TUMOR SUPPRESSOR PROTEINS; UBIQUITIN-PROTEIN LIGASES; VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN;

EID: 85047699831 PISSN: 09509232 EISSN: None Source Type: Journal
DOI: 10.1038/sj.onc.1205133 Document Type: Article

Times cited : (29)

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