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Volumn 43, Issue 1, 1996, Pages 109-114

Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas

Author keywords

Codon 768; Exon 13; Mutation; Pheochromocytoma; RET proto oncogene

Indexed keywords

ADULT; AGED; ARTICLE; CARCINOGENESIS; CODON; EXON; FEMALE; GENE MUTATION; HUMAN; HUMAN TISSUE; MALE; PHEOCHROMOCYTOMA; PROTO ONCOGENE;

EID: 0029932083     PISSN: 09188959     EISSN: None     Source Type: Journal    
DOI: 10.1507/endocrj.43.109     Document Type: Article
Times cited : (3)

References (19)
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    • Yoshimoto, K.1    Tanaka, C.2    Hamaguchi, S.3    Kimura, T.4    Iwahana, H.5    Miyauchi, A.6    Itakura, M.7
  • 10
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  • 13
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    • Kimura T, Yoshimoto K, Yokogoshi Y, Saito S (1995) Mutations in the cysteine-rich region of the RET proto-oncogene in patients diagnosed as having sporadic medullary thyroid carcinoma. Endocrine J 42: 517-525.
    • (1995) Endocrine J , vol.42 , pp. 517-525
    • Kimura, T.1    Yoshimoto, K.2    Yokogoshi, Y.3    Saito, S.4
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    • Current perspectives on the diagnosis and management of patients with multiple endocrine neoplasia type 2 syndromes
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.