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Volumn 156, Issue 2, 2000, Pages 651-659

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMAFFIN CELL; CHROMOSOME 1P; CHROMOSOME 3Q; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PRIORITY JOURNAL;

EID: 0033888981     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)64769-4     Document Type: Article
Times cited : (103)

References (32)
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  • 2
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    • (1997)
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    • Multiple endocrine neoplasia type 1: Clinical and genetic topics
    • (1998) Ann Intern Med , vol.129 , pp. 484-494
    • Marx, S.1
  • 7
    • 0008458244 scopus 로고    scopus 로고
    • The spectrum of mutations in MEN-1 variant syndromes
    • Program and Abstracts 80th Annual Meeting of Endocrine Society. New Orleans, LA, Endocrine Society, (abstract)
    • (1998) , pp. 106-107
    • Cote, G.J.1    Lee, J.E.2    Evans, D.B.3
  • 28
    • 0001014097 scopus 로고    scopus 로고
    • The European consortium on MEN1: Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
    • (1997) Hum Mol Genet , vol.7 , pp. 1177-1183


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.