메뉴 건너뛰기




Volumn 20, Issue 6, 2002, Pages 1480-1490

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: Analysis of 10,000 individuals

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BREAST CANCER; CANCER INVASION; CHILD; CLINICAL FEATURE; FAMILY HISTORY; FEMALE; GENE MUTATION; GENE SEQUENCE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; ONCOGENE; OVARY CANCER; PREVALENCE; PRIORITY JOURNAL; SEX;

EID: 0037087536     PISSN: 0732183X     EISSN: None     Source Type: Journal    
DOI: 10.1200/JCO.20.6.1480     Document Type: Article
Times cited : (787)

References (31)
  • 2
    • 0030662273 scopus 로고    scopus 로고
    • Human cancer syndromes: Clues to the origin and nature of cancer
    • (1997) Science , vol.278 , pp. 1043-1050
    • Fearon, E.R.1
  • 4
  • 14
  • 17
    • 0032565070 scopus 로고    scopus 로고
    • Frequency of breast cancer attributable to BRCA1 in a population-based series of American women
    • (1998) JAMA , vol.279 , pp. 915-921
    • Newman, B.1    Mu, H.2    Butler, L.M.3
  • 19
    • 0033818032 scopus 로고    scopus 로고
    • Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer
    • (2000) Hum Genet , vol.107 , pp. 186-191
    • Gao, Q.1    Tomlinson, G.2    Das, S.3
  • 22
    • 0032565074 scopus 로고    scopus 로고
    • BRCA1 mutations and breast cancer in the general population: Analyses in women before age 35 years and in women before age 45 years with first-degree family history
    • (1998) JAMA , vol.279 , pp. 922-929
    • Malone, K.E.1    Daling, J.R.2    Thompson, J.D.3
  • 26
    • 18244377693 scopus 로고    scopus 로고
    • Blinded comparison of methods for detecting germline BRCA1 mutations: Implications for molecular epidemiologic research and the practice of molecular medicine
    • (2001) J Med Genet , vol.38 , pp. 824-833
    • Eng, C.1    Brody, L.C.2    Wagner, T.M.U.3
  • 27
    • 0033799478 scopus 로고    scopus 로고
    • Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing
    • (2000) Am J Hum Genet , vol.67 , pp. 841-850
    • Unger, M.A.1    Nathanson, K.L.2    Calzone, K.3
  • 29
    • 0033909581 scopus 로고    scopus 로고
    • The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations
    • (2000) Am J Hum Genet , vol.67 , pp. 207-212


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.