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Volumn 126, Issue 10, 2006, Pages 2158-2159

Sebaceous skin lesions as clues to hereditary non-polyposis colorectal cancer

Author keywords

[No Author keywords available]

Indexed keywords

CANCER SUSCEPTIBILITY; COLORECTAL CANCER; FAMILY HISTORY; GENE MUTATION; HUMAN; IMMUNOHISTOCHEMISTRY; MICROSATELLITE INSTABILITY; MISMATCH REPAIR; MOLECULAR GENETICS; MUIR TORRE SYNDROME; PRIORITY JOURNAL; REVIEW; SEBACEOUS GLAND TUMOR;

EID: 33748759802     PISSN: 0022202X     EISSN: 15231747     Source Type: Journal    
DOI: 10.1038/sj.jid.5700534     Document Type: Note
Times cited : (15)

References (10)
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  • 4
    • 0019515269 scopus 로고
    • The cancer family syndrome: Rare cutaneous phenotypic linkage of Torre's syndrome
    • Lynch HT, Lynch PM, Pester J, Fusaro RM (1981) The cancer family syndrome: rare cutaneous phenotypic linkage of Torre's syndrome. Arch Intern Med 141:607-11
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    • 0014061877 scopus 로고
    • Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face
    • Muir EG, Bell AJ, Barlow KA (1967) Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face. Br J Surg 54:191-5
    • (1967) Br J Surg , vol.54 , pp. 191-195
    • Muir, E.G.1    Bell, A.J.2    Barlow, K.A.3
  • 6
    • 13944279163 scopus 로고    scopus 로고
    • Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: Role of clinical features, microsatellite instability and immunohistochemistry
    • Ponti G, Losi L, Di Gregorio C, Roncucci L, Pedroni M, Scarselli A et al. (2005) Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability and immunohistochemistry. Cancer 103:1018-25
    • (2005) Cancer , vol.103 , pp. 1018-1025
    • Ponti, G.1    Losi, L.2    Di Gregorio, C.3    Roncucci, L.4    Pedroni, M.5    Scarselli, A.6
  • 7
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    • Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas
    • Ponti G, Losi L, Pedroni M, Lucci-Cordisco E, Di Gregorio C, Pellacani G et al. (2006) Value of MLH1 and MSH2 mutations in the appearance of Muir-Torre syndrome phenotype in HNPCC patients presenting sebaceous gland tumors or keratoacanthomas. J Invest Dermatol 126:2302-2307
    • (2006) J Invest Dermatol , vol.126 , pp. 2302-2307
    • Ponti, G.1    Losi, L.2    Pedroni, M.3    Lucci-Cordisco, E.4    Di Gregorio, C.5    Pellacani, G.6
  • 8
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    • Multiple sebaceous tumors
    • Torre D (1968) Multiple sebaceous tumors. Arch Dermatol 98:549-51
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  • 9
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    • Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
    • Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J et al. (2004) Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96:261-8
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  • 10
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    • Heredity with reference to carcinoma as shown by the study of the cases examined in the pathological laboratory of the University of Michigan, 1895-1913
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    • Warthin, A.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.