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Volumn 22, Issue SUPPL., 2009, Pages

Familial atypical multiple mole melanoma syndrome - FAMMM;Syndrom familiárního melanomu (s dysplastickými naevy či bez nich)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE 4; CYCLIN DEPENDENT KINASE INHIBITOR 2A;

EID: 67650921129     PISSN: 0862495X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey
Times cited : (3)

References (15)
  • 5
    • 0034161312 scopus 로고    scopus 로고
    • Germline CDKN2A mutation implicated in predisposition to multiple myeloma
    • Dilworth D, Liu L, Stewart K et al. Germline CDK2A mutations implicated in predisposition to multiple myeloma. Blood 2000; 95(5): 1869-1871. (Pubitemid 30120855)
    • (2000) Blood , vol.95 , Issue.5 , pp. 1869-1871
    • Dilworth, D.1    Liu, L.2    Stewart, A.K.3    Berenson, J.R.4    Lassam, N.5    Hogg, D.6
  • 6
    • 2142645979 scopus 로고    scopus 로고
    • Clinical germline genetic testing for melanoma
    • DOI 10.1016/S1470-2045(04)01469-X, PII S147020450401469X
    • Hansen CB, Wadge LM, Lowstuter K et al. Clinical germline genetic testing for melanoma. The Lancet Oncology 2004; 5: 314-319. (Pubitemid 38541583)
    • (2004) Lancet Oncology , vol.5 , Issue.5 , pp. 314-319
    • Hansen, C.B.1    Wadge, L.M.2    Lowstuter, K.3    Boucher, K.4    Leachman, S.A.5
  • 8
    • 0037311133 scopus 로고    scopus 로고
    • Contribution of germline mutations in BRCA2, p16INK4A, p14 and p15 to uveal melanoma
    • Hearle N, Damato BE, Humphreys J. Contribution of germline mutations in BRCA2, p16INK4A, p14 and p15 to uveal melanoma. Investigative Ophtalmology and Visual Science 2003; 44(2): 458-462.
    • (2003) Investigative Ophtalmology and Visual Science , vol.44 , Issue.2 , pp. 458-462
    • Hearle, N.1    Damato, B.E.2    Humphreys, J.3
  • 11
    • 0142186728 scopus 로고    scopus 로고
    • Identification of a splice acceptor site mutation in p16INK4A/p14ARF within a breast cancer, melanoma, neurofibroma prone kindreds
    • Prowse AH, Schultz DC, Guo S et al. Identification of a splice acceptor site mutation in p16INK4A/p14ARF within a breast cancer, melanoma, neurofibroma prone kindreds. J Med Genet 2003; 40: 1-7.
    • (2003) J Med Genet , vol.40 , pp. 1-7
    • Prowse, A.H.1    Schultz, D.C.2    Guo, S.3
  • 15
    • 84888557234 scopus 로고    scopus 로고
    • www.genomel.org


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.