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Pediatric Blood and Cancer
Volumn 44, Issue 3, 2005, Pages 289-
Neurofibromatosis type 1 and multiple primary malignancies [1]
Author keywords

[No Author keywords available]
Indexed keywords

BRAIN TUMOR; COLORECTAL ADENOMA; COLORECTAL CANCER; FAMILY HISTORY; GENE MUTATION; HEMATOLOGIC MALIGNANCY; HUMAN; LETTER; LEUKEMIA; LYMPHOMA; MISMATCH REPAIR; MUIR TORRE SYNDROME; MULTIPLE CANCER; NEUROFIBROMATOSIS; PHENOTYPE; PRIORITY JOURNAL; TURCOT SYNDROME;
EID: 13444260740     PISSN: 15455009     EISSN: None     Source Type: Journal    
DOI: 10.1002/pbc.20197     Document Type: Letter
Times cited : (2)
References (3)
  • 1
    • 0242490564 scopus 로고    scopus 로고
    • Neurofibromatosis type 1 and multiple primary malignancies
    • Barbaric D, Stevens M, Dalla-Pozza L. Neurofibromatosis type 1 and multiple primary malignancies. Med Pediatr Oncol 2003;41: 568-569.
    • (2003) Med Pediatr Oncol , vol.41 , pp. 568-569
    • Barbaric, D.1    Stevens, M.2    Dalla-Pozza, L.3
  • 2
    • 0035770411 scopus 로고    scopus 로고
    • Cafe-au-lait spots and early onset colorectal neoplasia: A variant of HNPCC?
    • Trimbath JD, Petersen GM, Erdman SH, et al. Cafe-au-lait spots and early onset colorectal neoplasia: A variant of HNPCC? Familial Cancer 2001;1:101-105.
    • (2001) Familial Cancer , vol.1 , pp. 101-105
    • Trimbath, J.D.1    Petersen, G.M.2    Erdman, S.H.3
  • 3
    • 0037081077 scopus 로고    scopus 로고
    • A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots
    • Whiteside D, McLeod R, Graham G, et al. A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots. Cancer Res 2002;62: 359-362.
    • (2002) Cancer Res , vol.62 , pp. 359-362
    • Whiteside, D.1    McLeod, R.2    Graham, G.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.