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Volumn 59, Issue 2, 1999, Pages 455-461

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST CANCER; CANCER RISK; CAUCASIAN; EXON; FAMILY STUDY; FEMALE; GENE DELETION; GENE REARRANGEMENT; GENETIC PREDISPOSITION; GENETIC SCREENING; HETEROZYGOTE DETECTION; HUMAN; MAJOR CLINICAL STUDY; ONCOGENE; PRIORITY JOURNAL; PROMOTER REGION; SCREENING TEST;

EID: 0033556051     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (150)

References (30)
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    • Smith, T. M., Lee, M. K., Szabo, C. I., Jerome, N., McEuen, M., Taylor, M., Hood, L., and King, M. C. Complete genomic sequence and analysis of 117 kb of human DNA containing the gene KRCA1. Genome Res., 6: 1029-1049, 1996.
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  • 13
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    • Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
    • Friedman, L. S., Ostermeyer, E. A., Szabo, C. I.. Dowd, P., Lynch, E. D., Rowell, S. E., and King, M-C. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat. Genet., 8: 399-404, 1994.
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    • Xu, C.-F.1    Brown, M.A.2    Nicolai, H.3    Chambers, J.A.4    Griffiths, B.L.5    Solomon, E.6
  • 19
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    • Germline mutations in the von HippelLindau disease (VHL) gene in Japanese VHL
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.