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Volumn 99, Issue 11, 2010, Pages 1741-1743

Fanconi anaemia, BRCA2 and familial considerations - Follow up on a previous case report

Author keywords

[No Author keywords available]

Indexed keywords

BRCA2 PROTEIN;

EID: 84988290452     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2010.01929.x     Document Type: Article
Times cited : (4)

References (8)
  • 1
    • 0034967468 scopus 로고    scopus 로고
    • Microcephalus, medulloblastoma and excessive toxicity from chemotherapy: An unusual presentation of Fanconi anemia
    • Ruud E, Wesenberg F. Microcephalus, medulloblastoma and excessive toxicity from chemotherapy: An unusual presentation of Fanconi anemia. Acta Paediatr 2001; 90: 580-3.
    • (2001) Acta Paediatr , vol.90 , pp. 580-583
    • Ruud, E.1    Wesenberg, F.2
  • 4
    • 11144353924 scopus 로고    scopus 로고
    • Germline mutations in BRCA2: Shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia
    • Wagner JE, Tolar J, Levran O, Scholl T, Deffenbaugh A, Satagopan J, et al. Germline mutations in BRCA2: Shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. Blood 2004; 103: 3226-9.
    • (2004) Blood , vol.103 , pp. 3226-3229
    • Wagner, J.E.1    Tolar, J.2    Levran, O.3    Scholl, T.4    Deffenbaugh, A.5    Satagopan, J.6
  • 6
    • 49649087897 scopus 로고    scopus 로고
    • Classifying variants of undetermined significance in BRCA2 with protein likelihood ratios
    • Karchin R, Agarwal M, Sali A, Couch F, Beattie MS. Classifying variants of undetermined significance in BRCA2 with protein likelihood ratios. Cancer Inform 2008; 6: 203-16.
    • (2008) Cancer Inform , vol.6 , pp. 203-216
    • Karchin, R.1    Agarwal, M.2    Sali, A.3    Couch, F.4    Beattie, M.S.5
  • 7
    • 33846415079 scopus 로고    scopus 로고
    • Clinical and molecular features associated with biallelic mutations in FANCD1/ BRCA2
    • Alter BP, Rosenberg PS, Brody LC. Clinical and molecular features associated with biallelic mutations in FANCD1/ BRCA2. J Med Genet 2007; 44: 1-9.
    • (2007) J Med Genet , vol.44 , pp. 1-9
    • Alter, B.P.1    Rosenberg, P.S.2    Brody, L.C.3
  • 8
    • 34447298637 scopus 로고    scopus 로고
    • Genetic epidemiology of BRCA mutations-family history detects less than 50% of the mutation carriers
    • Møller P, Hagen AI, Apold J, Mæhle L, Clark N, Fiane B, et al. Genetic epidemiology of BRCA mutations-family history detects less than 50% of the mutation carriers. Eur J Cancer 2007; 43: 1713-7.
    • (2007) Eur J Cancer , vol.43 , pp. 1713-1717
    • Møller, P.1    Hagen, A.I.2    Apold, J.3    Mæhle, L.4    Clark, N.5    Fiane, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.