共 16 条
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White J.C., Multiple benign cystic epitheliomas, J Cutan Genitourin Dis, 12, pp. 477-484, (1894)
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Bare J.W., Lebo R.V., Epstein E.H., Loss of heterozygosity at chromosome 1q22 in basal cell carcinomas and exclusion of the Basal cell nevus syndrome gene from this site, Cancer Res, 52, pp. 1494-1498, (1992)
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Bialer M.G., Gailani M.R., McLaughlin J.A., Petrikovsky B., Bale A.E., Prenatal Diagnosis of Gorlin syndrome, Lancet, 344, (1994)
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Bonifas J.M., Bare J.W., Kerschmann R.L., Master S.P., Epstein E.H., Parental origin of chromosome 9q22.3-q31 lost in basal cell Carcinomas from basal cell nevus syndrome patients, Hum Mol Genet, 3, (1994)
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Farndon P.A., Del Mastro R.G., Evans D.G., Kilpatrick M.W., Location of Gene for Gorlin syndrome, Lancet, 339, pp. 581-582, (1992)
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Evans D.G., Birch J.M., Orton C.I., Brain tumours and the occurrence of severe invasive basal cell carcinoma in first degree Relatives with Gorlin syndrome, Br J Neurosurg, 5, pp. 643-646, (1991)
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Pratt M.D., Jackson R., Nevoid basal cell carcinoma syndrome. A 15-year follow-up of cases in Ottawa and the Ottawa Valley, J Am Acad Dermatol, 16, pp. 964-970, (1987)
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Lo Muzio L., Nocini P.F., Savoia A., Consolo U., Procaccini M., Zelante L., Pannone G., Bucci P., Dolci M., Bambini F., Et al., Nevoid basal cell Carcinoma syndrome. Clinical findings in 37 Italian affected individuals, Clin Genet, 55, pp. 34-40, (1999)