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Volumn 110, Issue 3, 2004, Pages 320-325

Limited relevance of the CHEK2 gene in hereditary breast cancer

Author keywords

BRCA1; BRCA2; Breast cancer; CHEK2; Mutation analysis

Indexed keywords

BRCA2 PROTEIN; CHECKPOINT KINASE 2;

EID: 2442476240     PISSN: 00207136     EISSN: None     Source Type: Journal    
DOI: 10.1002/ijc.20073     Document Type: Article
Times cited : (79)

References (21)
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    • Analysis of CHEK2 1100delC in North American breast cancer families and population based breast cancer series
    • Walsh T, Young T-L, Snook S, Newman B, Milikan B, N.Y.B.C.S. Consortium, Laing K, Green J, King M-C. Analysis of CHEK2 1100delC in North American breast cancer families and population based breast cancer series. Am J Hum Genet 2002;71(Suppl):90.
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    • Walsh, T.1    Young, T.-L.2    Snook, S.3    Newman, B.4    Milikan, B.5    Laing, K.6    Green, J.7    King, M.-C.8
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    • Falck, J.1    Mailand, N.2    Syljuasen, R.G.3    Bartek, J.4    Lukas, J.5
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    • Functional impact of concomitant versus alternative defects in the Chk2-p53 tumour suppressor pathway
    • Falck J, Lukas C, Protopopova M, Lukas J, Selivanova C, Bartek J. Functional impact of concomitant versus alternative defects in the Chk2-p53 tumour suppressor pathway. Oncogene 2001;20:5503-10.
    • (2001) Oncogene , vol.20 , pp. 5503-5510
    • Falck, J.1    Lukas, C.2    Protopopova, M.3    Lukas, J.4    Selivanova, C.5    Bartek, J.6
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.