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Volumn 21, Issue 3, 1998, Pages 244-249

Identification of missense and truncating mutations in the BRCA1 gene in sporadic and familial breast and ovarian cancer

Author keywords

[No Author keywords available]

Indexed keywords

HETERODUPLEX;

EID: 0031905512     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1098-2264(199803)21:3<244::aid-gcc9>3.0.co;2-%23     Document Type: Article
Times cited : (28)

References (24)
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    • Abeliovich D, Kaduri L, Lerer I, Weinberg N, Amir G, Sagi M, Zlotogora J, Heching N, Peretz T (1997) The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women. Am J Hum Genet 60:505-514.
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    • Transcriptional activation by BRCA1
    • Chapman MS, Verma IM (1996) Transcriptional activation by BRCA1. Nature 382:678-679.
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    • The genetic attributable risk of breast and ovarian cancer
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    • Couch, F.J.1    Weber, B.L.2    Core, B.C.I.3
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    • Durocher F, Shattuck-Eidens D, McClure M, Labrie F, Skolnick MH, Goldgar DE, Simard J (1996) Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations. Hum Mol Genet 5:835-842.
    • (1996) Hum Mol Genet , vol.5 , pp. 835-842
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  • 9
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    • Ford D, Easton DF, Peto J (1995) Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet 57:1457-1462.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.