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Volumn 45, Issue 3, 2006, Pages 213-219

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: A possible hot spot?

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADRENAL MEDULLA; ADULT; AGED; ARTICLE; CLINICAL ARTICLE; EXON; FEMALE; GENE DELETION; GENETIC ANALYSIS; HUMAN; INHERITANCE; MALE; MULTIPLEX POLYMERASE CHAIN REACTION; NEUROENDOCRINE TUMOR; NF1 GENE; ONCOGENE; ONCOGENE RET; PARAGANGLIOMA; PHEOCHROMOCYTOMA; POINT MUTATION; PRIORITY JOURNAL; SCHOOL CHILD; SDHB GENE; SDHC GENE; SDHD GENE; TUMOR LOCALIZATION; VHL GENE;

EID: 32544439562     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/gcc.20283     Document Type: Article
Times cited : (67)

References (18)
  • 1
    • 0027395614 scopus 로고
    • Familial risk for neuroendocrine tumors
    • Anderson RJ, Lynch HT. 1993. Familial risk for neuroendocrine tumors. Curr Opin Oncol 5:75-84.
    • (1993) Curr Opin Oncol , vol.5 , pp. 75-84
    • Anderson, R.J.1    Lynch, H.T.2
  • 5
    • 6044230918 scopus 로고    scopus 로고
    • Molecular profiling of inflammatory breast cancer: Identification of a poor-prognosis gene expression signature
    • Bieche I, Lerebours F, Tozlu S, Espie M, Marty M, Lidereau R. 2004. Molecular profiling of inflammatory breast cancer: identification of a poor-prognosis gene expression signature. Clin Cancer Res 10:6789-6795.
    • (2004) Clin Cancer Res , vol.10 , pp. 6789-6795
    • Bieche, I.1    Lerebours, F.2    Tozlu, S.3    Espie, M.4    Marty, M.5    Lidereau, R.6
  • 8
    • 0036778597 scopus 로고    scopus 로고
    • The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors
    • Kolomietz E, Meyn MS, Pandita A, Squire JA. 2002. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors. Genes Chromosomes Cancer 35:97-112.
    • (2002) Genes Chromosomes Cancer , vol.35 , pp. 97-112
    • Kolomietz, E.1    Meyn, M.S.2    Pandita, A.3    Squire, J.A.4
  • 14
    • 0033767445 scopus 로고    scopus 로고
    • Mutations in SDHC cause autosomal dominant paraganglioma, type 3
    • Niemann S, Muller U. 2000. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 26:268-270.
    • (2000) Nat Genet , vol.26 , pp. 268-270
    • Niemann, S.1    Muller, U.2
  • 16
    • 0025081167 scopus 로고
    • Multiple endocrine neoplasia: How many syndromes?
    • Schimke RN. 1990. Multiple endocrine neoplasia: how many syndromes? Am J Med Genet 37:375-383.
    • (1990) Am J Med Genet , vol.37 , pp. 375-383
    • Schimke, R.N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.