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Volumn 58, Issue 5, 1998, Pages 863-866

An interstitial tandem duplication of 9p23-24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer

Author keywords

[No Author keywords available]

Indexed keywords

BRCA2 PROTEIN;

EID: 0032031074     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (20)

References (26)
  • 1
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    • Schottenfeld, D.1    Lilienfeld, A.M.2    Diamond, H.3
  • 4
    • 0023780504 scopus 로고
    • Endocrine epidemiology of male breast cancer
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    • Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
    • Gayther, S. A., Mangion, J., Russel, P., Seal, S., Barfoot, R., Ponder, B. A., Stratton, M. R., and Easton, D. Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. Nat. Genet., 15: 103-105, 1997.
    • (1997) Nat. Genet. , vol.15 , pp. 103-105
    • Gayther, S.A.1    Mangion, J.2    Russel, P.3    Seal, S.4    Barfoot, R.5    Ponder, B.A.6    Stratton, M.R.7    Easton, D.8
  • 17
    • 0030902559 scopus 로고    scopus 로고
    • BRCA2 in American families with four or more cases of breast or ovarian cancer: Recurrent and novel mutations, variable expression, penetrance and the possibility of families whose breast cancer is not attributable to BRCA1 or BRCA2
    • Schubert, E. L., Lee, M. K., Mefford, H. C., Argonza, R. H., Morrow, J. E., Hull, J., Dann, J. L., and King, M-C. BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance and the possibility of families whose breast cancer is not attributable to BRCA1 or BRCA2. Am. J. Hum. Genet., 60: 1031-1040, 1997.
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 1031-1040
    • Schubert, E.L.1    Lee, M.K.2    Mefford, H.C.3    Argonza, R.H.4    Morrow, J.E.5    Hull, J.6    Dann, J.L.7    King, M.-C.8
  • 20
    • 0028023048 scopus 로고
    • Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells
    • Savelyeva, L., Corvi, R., and Schwab, M. Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells. Am. J. Hum. Genet., 55: 334-340, 1994.
    • (1994) Am. J. Hum. Genet. , vol.55 , pp. 334-340
    • Savelyeva, L.1    Corvi, R.2    Schwab, M.3
  • 21
    • 0028305310 scopus 로고
    • MYCN is retained in single copy at chromosome band 2p23-24 during amplification in human neuroblastoma cells
    • Corvi, R., Amler, L. C., Savelyeva, L., Gehring, M., and Schwab, M. MYCN is retained in single copy at chromosome band 2p23-24 during amplification in human neuroblastoma cells. Proc. Natl. Acad. Sci. USA, 91: 5523-5527, 1994.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 5523-5527
    • Corvi, R.1    Amler, L.C.2    Savelyeva, L.3    Gehring, M.4    Schwab, M.5
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    • Constitutive heterochromatin studies in patients with solid tumors
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    • Suciu, S.1
  • 25
    • 0028060062 scopus 로고
    • Molecular cytogenetic characterization of two types of chromosome 9 variants
    • Wang, J-C. C., and Miller, W. A. Molecular cytogenetic characterization of two types of chromosome 9 variants. Cytogenet. Cell Genet., 67: 190-192, 1994.
    • (1994) Cytogenet. Cell Genet. , vol.67 , pp. 190-192
    • Wang, J.-C.C.1    Miller, W.A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.