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0019497899
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Genetics of Wilms' tumor
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Mutation and cancer: A model for Wilms' tumor of the kidney
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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
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Call, K. M., Glaser, T., Ito, C. Y., Buckler, A. J., Pelletier, J., Haber, D. A. Rose, E. A., Kral, A., Yeger, H., Lewis, W. H., Jones C., and Housman, D. E. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell. 60: 509-520, 1990.
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4
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0025098654
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Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping
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Gessler, M., Poustka, A., Cavenee, W., Neve, R. L., Orkin, S. H., and Bruns, G. A. P. Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping. Nature (Lond.), 343: 774-778, 1990.
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5
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0023803361
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Lack of linkage of familial Wilms' tumour to chromosomal band 11p13
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Huff, V., Compton, D. A., Chao, L., Strong, L. C., Geiser, C. F., and Saunders, G. F. Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature (Lond.), 336: 377-378, 1988.
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6
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0023683531
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Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
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Grundy, P., Koufos, A., Morgan, K., Li, F. P., Meadows, A. T., and Cavenee, W. K. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature (Lond.), 336: 374-376, 1988.
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0025826538
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Familial predisposition to Wilms' tumor does not segregate with the WT1 gene
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Schwartz, C. E., Haber, D. A., Stanton, V. P., Strong, L. C., Skolnick, M. H., and Housman, D. E. Familial predisposition to Wilms' tumor does not segregate with the WT1 gene. Genomics, 10: 927-930, 1991.
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8
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0030017174
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Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21
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Rahman, N., Arbour, L., Tonin, P., Renshaw, J., Pelletier. J., Baruchel, S., PritchardJones, K., Stratton, M. R., and Narod, S. A. Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21. Nat. Genet., 13: 461-462, 1996.
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9
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Evidence for genetic heterogeneity in familial Wilms' tumor
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Huff, V., Douglass, E. C., Fisher, R., Geiser, C. F., Krill, C. E., Li, F. P., Strong, L. C., and McDonald, J. M. Evidence for genetic heterogeneity in familial Wilms' tumor. Cancer Res., 57: 1859-1862, 1997.
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10
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Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11
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Mannens, M., Devilee, P., Bliek, J., Mandjes, I., de Kraker, J., Heyting, C., Slater, R. M., and Westerveld, A. Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Res., 50: 3279-3283, 1990.
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11
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0026691721
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A third Wilms' tumor locus on chromosome 16q
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Maw, M. A., Grundy, P. E., Millow, L. J., Eccles, M. R., Dunn, R. S., Smith, P. J., Feinberg, A. P., Law, D. J., Paterson, M. C, Telzerow, P. E., Callen, D. F., Thompson. A. D., Richards, R. I., and Reeve, A. E. A third Wilms' tumor locus on chromosome 16q. Cancer Res., 52: 3094-3098, 1992.
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12
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0026457965
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Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
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Huff, V., Reeve, A. E., Leppert, M., Strong, L. C., Douglass, E. C., Geiser, C. F., Li, F. P., Meadows, A., Callen, D. F., Lenoir, G., and Saunders, G. F. Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Cancer Res., 52: 6117-6120, 1992.
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13
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0016302483
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Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies
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Cottingham, R. W., Jr., Idury, R. M., and Schaffer, A. A. Faster sequential genetic linkage computations. Am. J. Hum. Genet., 53: 252-263, 1993.
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Estimating the power of a proposed linkage study for a complex genetic trait
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Epidemiology of Wilms' tumor
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Hereditary multiple exostosis and chondrosarcoma: Linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8
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Hecht, J. T., Hogue, D., Strong, L. C., Hansen, M. F., Blanton, S. H., and Wagner, M. Hereditary multiple exostosis and chondrosarcoma: linkage to chromosome 11 and loss of heterozygosity for EXT-linked markers on chromosomes 11 and 8. Am. J. Hum. Genet., 56: 1125-1131, 1995.
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19
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Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25
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McIndoe, R. A., Stanford, J. L., Gibbs, M., Jarvik, G. P., Brandzel, S., Neal, C. L., Li, S., Gammack, J. T., Gay, A. A., Goode, E. L., Hood, L., and Ostrander, E. A. Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at 1q24-25. Am. J. Hum. Genet., 61: 347-353, 1997.
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A metric map of humans: 23,500 loci in 850 bands
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