Genetics of the nevoid basal cell carcinoma syndrome.
暂无分享,去创建一个
[1] Michael Dean,et al. Mutations of the Human Homolog of Drosophila patched in the Nevoid Basal Cell Carcinoma Syndrome , 1996, Cell.
[2] I. Vořechovský,et al. A Mammalian patched Homolog Is Expressed in Target Tissues of sonic hedgehog and Maps to a Region Associated with Developmental Abnormalities (*) , 1996, The Journal of Biological Chemistry.
[3] Wei-Jen Tang,et al. Two Cytoplasmic Domains of Mammalian Adenylyl Cyclase Form a G- and Forskolin-activated Enzyme in Vitro(*) , 1996, The Journal of Biological Chemistry.
[4] B. Wold,et al. Know Your Neighbors: Three Phenotypes in Null Mutants of the Myogenic bHLH Gene MRF4 , 1996, Cell.
[5] Cécile Fizames,et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites , 1996, Nature.
[6] L. Donahue,et al. Mesenchymal dysplasia: a recessive mutation on chromosome 13 of the mouse. , 1996, The Journal of heredity.
[7] Kenneth H. Kraerner. Are people who get skin cancer different , 1995 .
[8] G. Neri,et al. Further contribution to the description of phenotypes associated with partial 4q duplication. , 1995, American journal of medical genetics.
[9] D. Leffell,et al. Nevoid basal cell carcinoma syndrome. , 1994, The Journal of investigative dermatology.
[10] A. Goldstein,et al. Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q. , 1994, The Journal of investigative dermatology.
[11] G. Chenevix-Trench,et al. Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome. , 1994, Genomics.
[12] A. Goldstein,et al. Localization of the gene for the nevoid basal cell carcinoma syndrome. , 1994, American journal of human genetics.
[13] A. Goldstein,et al. Clinical findings in two African-American families with the nevoid basal cell carcinoma syndrome (NBCC). , 1994, American journal of medical genetics.
[14] E. Haan,et al. Nevoid basal cell carcinoma syndrome: review of 118 affected individuals. , 1994, American journal of medical genetics.
[15] E. Healy,et al. Chromosome 9 allele loss occurs in both basal and squamous cell carcinomas of the skin. , 1994, The Journal of investigative dermatology.
[16] O. Wiestler,et al. Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11 p and 17p in medulloblastomas , 1994, Neuropathology and applied neurobiology.
[17] M. Cohen,et al. Encephalocraniocutaneous lipomatosis, Proteus syndrome, and somatic mosaicism. , 1993, American journal of medical genetics.
[18] M. Cohen,et al. Proteus syndrome: clinical evidence for somatic mosaicism and selective review. , 1993, American journal of medical genetics.
[19] E. Haan,et al. Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity. , 1993, American journal of human genetics.
[20] N. Carter,et al. Multiple self–healing squamous epitheliomata (ESS1) mapped to chromosome 9q22–q31 in families with common ancestry , 1993, Nature Genetics.
[21] M. Greene,et al. Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9 , 1992, Cell.
[22] D. Evans,et al. Location of gene for Gorlin syndrome , 1992, The Lancet.
[23] R. Wegner,et al. Localisation of gene for the naevoid basal-cell carcinoma syndrome , 1992, The Lancet.
[24] D. Evans,et al. The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma. , 1991, British Journal of Cancer.
[25] W. Sahl. Familial nevus sebaceus of Jadassohn: occurrence in three generations. , 1990, Journal of the American Academy of Dermatology.
[26] D. Viljoen,et al. Cutaneous Manifestations of the Proteus Syndrome , 1988, Pediatric dermatology.
[27] Robert J. Gorlin,et al. Nevoid Basal‐Cell Carcinoma Syndrome , 1987, Medicine.
[28] J. Springate. The nevoid basal cell carcinoma syndrome. , 1986, Journal of pediatric surgery.
[29] J. Howell,et al. Commentary: The Nevoid Basal Cell Carcinoma Syndrome , 1982 .
[30] Li Yang,et al. Tumors of the Skin , 1980 .
[31] L. Strong. Genetic and environmental interactions , 1977, Cancer.
[32] A. Knudson. Mutation and cancer: statistical study of retinoblastoma. , 1971, Proceedings of the National Academy of Sciences of the United States of America.
[33] J. Block,et al. BASAL CELL NEVUS SYNDROME. , 1964, Archives of dermatology.
[34] J. J. Pollard,et al. Hereditary Cutaneomandibular Polyoncosis , 1964 .
[35] R. Winkelmann,et al. Multiple Nevoid Basal Cell Epitheliomas, Jaw Cysts, and Skeletal Defects: A Clinical Syndrome , 1964 .
[36] W. Ward,et al. NÆVOID BASAL CELLED CAECINOMA ASSOCIATED WITH A DYSKERATOSIS OF THE PALMS AND SOLES. * A NEW ENTITY , 1960, Australian journal of dermatology.
[37] R. Gorlin,et al. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. , 1960, The New England journal of medicine.
[38] R. Nomland. MULTIPLE BASAL CELL EPITHELIOMAS ORIGINATING FROM CONGENITAL PIGMENTED BASAL CELL NEVI , 1932 .
[39] S. Povey,et al. Comparative mapping of 50 human chromosome 9 loci in the laboratory mouse. , 1995, Genomics.
[40] G. Chenevix-Trench,et al. Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas. , 1995, Human molecular genetics.
[41] M. Rutter,et al. A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig. , 1995, Genomics.
[42] J. Howell,et al. The basal-cell nevus: its relationship to multiple cutaneous cancers and associated anomalies of development. , 1959, A.M.A. archives of dermatology.