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Volumn 98, Issue 6, 1996, Pages 747-750

Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASE MISPAIRING; CASE REPORT; COLORECTAL CANCER; GENE; GENE MUTATION; GERM LINE; HUMAN; HUMAN TISSUE; MALE; PRIORITY JOURNAL; SKIN TUMOR;

EID: 10544255347     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050298     Document Type: Article
Times cited : (60)

References (18)
  • 2
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    • Association of sebaceous gland tumors and internal malignancy: The Muir-Torre syndrome
    • Cohen PR, Kohn SR, Kurzrock R (1991) Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome. Am J Med 90:606-613
    • (1991) Am J Med , vol.90 , pp. 606-613
    • Cohen, P.R.1    Kohn, S.R.2    Kurzrock, R.3
  • 3
    • 0027171303 scopus 로고
    • Single-step screening method for the most common mutations in familial adenomatous polyposis
    • Friedl W, Mandl M, Sengteller M (1993) Single-step screening method for the most common mutations in familial adenomatous polyposis. Hum Mol Genet 2:1481-1482
    • (1993) Hum Mol Genet , vol.2 , pp. 1481-1482
    • Friedl, W.1    Mandl, M.2    Sengteller, M.3
  • 13
    • 0022006650 scopus 로고
    • Muir-Torre syndrome in several members of a family with a variant of the cancer family syndrome
    • Lynch HT, Fusaro RM, Roberts L, Voorhees GJ, Lynch JF (1985) Muir-Torre syndrome in several members of a family with a variant of the cancer family syndrome. Br J Dermatol 113:295-301
    • (1985) Br J Dermatol , vol.113 , pp. 295-301
    • Lynch, H.T.1    Fusaro, R.M.2    Roberts, L.3    Voorhees, G.J.4    Lynch, J.F.5
  • 14
    • 0028091285 scopus 로고
    • Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis
    • Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P (1994) Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis. Hum Mol Genet 3:181-184
    • (1994) Hum Mol Genet , vol.3 , pp. 181-184
    • Mandl, M.1    Paffenholz, R.2    Friedl, W.3    Caspari, R.4    Sengteller, M.5    Propping, P.6
  • 15
    • 0029013597 scopus 로고
    • The Muir-Torre syndrome: A 25-year retrospect
    • Schwartz RA, Torre DP (1995) The Muir-Torre syndrome: a 25-year retrospect. J Am Acad Dermatol 33:90-104
    • (1995) J Am Acad Dermatol , vol.33 , pp. 90-104
    • Schwartz, R.A.1    Torre, D.P.2
  • 16
    • 0025848680 scopus 로고
    • The International Collaborative Group on hereditary non-polyposis colorectal cancer
    • Vasen HFA, Mecklin J-P, Meera Khan P, Lynch HT (1991) The International Collaborative Group on hereditary non-polyposis colorectal cancer. Dis Colon Rectum 34:424-425
    • (1991) Dis Colon Rectum , vol.34 , pp. 424-425
    • Vasen, H.F.A.1    Mecklin, J.-P.2    Meera Khan, P.3    Lynch, H.T.4
  • 18
    • 8544252126 scopus 로고    scopus 로고
    • Hereditary non-polyposis colorectal cancer (HNPCC): Eight novel germline mutations in the hMSH2 or hMLH1 genes
    • in press
    • Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W (1996) Hereditary non-polyposis colorectal cancer (HNPCC): eight novel germline mutations in the hMSH2 or hMLH1 genes. Hum Mutat (in press)
    • (1996) Hum Mutat
    • Wehner, M.1    Buschhausen, L.2    Lamberti, C.3    Kruse, R.4    Caspari, R.5    Propping, P.6    Friedl, W.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.