-
1
-
-
0026907525
-
Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
-
Baird, P. N., Santos, A., Groves, N., Jadresic, L., and Cowell, J. K. (1992). Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome. Hum. Mol. Genet. 1: 301-305.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 301-305
-
-
Baird, P.N.1
Santos, A.2
Groves, N.3
Jadresic, L.4
Cowell, J.K.5
-
2
-
-
0025695815
-
Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts
-
Bonetta, L., Kuehn, S. E., Huang, A., Law, D. J., Kalikin, L. M., Koi, M., Reeve, A. E., Brownstein, B. H., Yeger, H., Williams, B. R. G., and Feinberg, A. P. (1990). Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts. Science 250: 994-997.
-
(1990)
Science
, vol.250
, pp. 994-997
-
-
Bonetta, L.1
Kuehn, S.E.2
Huang, A.3
Law, D.J.4
Kalikin, L.M.5
Koi, M.6
Reeve, A.E.7
Brownstein, B.H.8
Yeger, H.9
Williams, B.R.G.10
Feinberg, A.P.11
-
3
-
-
0027420317
-
Low frequency of mutations in the WT1 coding region in Wilms' tumor
-
Brown, K. W., Wilmore, H. P., Watson, J. E., Mott, M. G., Berry, P. J., and Maitland, N. J. (1993). Low frequency of mutations in the WT1 coding region in Wilms' tumor. Genes Chromosomes Cancer 8: 74-79.
-
(1993)
Genes Chromosomes Cancer
, vol.8
, pp. 74-79
-
-
Brown, K.W.1
Wilmore, H.P.2
Watson, J.E.3
Mott, M.G.4
Berry, P.J.5
Maitland, N.J.6
-
4
-
-
0026864939
-
Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development
-
Bruening, W., Bardeesy, N., Silverman, B. L., Cohn, R. A., Machin, G. A., Aronson, A. J., Housman, D., and Pelletier, J. (1992). Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. Nature Genet. 1: 144-148.
-
(1992)
Nature Genet.
, vol.1
, pp. 144-148
-
-
Bruening, W.1
Bardeesy, N.2
Silverman, B.L.3
Cohn, R.A.4
Machin, G.A.5
Aronson, A.J.6
Housman, D.7
Pelletier, J.8
-
5
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
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. (1990). Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60: 509-520.
-
(1990)
Cell
, vol.60
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
Buckler, A.J.4
Pelletier, J.5
Haber, D.A.6
Rose, E.A.7
Kral, A.8
Yeger, H.9
Lewis, W.H.10
Jones, C.11
Housman, D.E.12
-
6
-
-
0027465535
-
Genetic mosaicism in normal tissues of Wilms' tumour patients
-
Chao, L.-Y., Huff, V., Tomlinson, G., Riccardi, V. M., Strong, L. C., and Saunders, G. F. (1993). Genetic mosaicism in normal tissues of Wilms' tumour patients. Nature Genet. 3: 127-131.
-
(1993)
Nature Genet.
, vol.3
, pp. 127-131
-
-
Chao, L.-Y.1
Huff, V.2
Tomlinson, G.3
Riccardi, V.M.4
Strong, L.C.5
Saunders, G.F.6
-
7
-
-
0026685962
-
Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination
-
Coppes, M. J., Bonetta, L., Huang, A., Hoban, P., Chilton-MacNeill, S., Campbell, C. E., Weksberg, R., Yeger, H., Reeve, A. E., and Williams, B. R. G. (1992a). Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes Chromosomes Cancer 5: 326-334.
-
(1992)
Genes Chromosomes Cancer
, vol.5
, pp. 326-334
-
-
Coppes, M.J.1
Bonetta, L.2
Huang, A.3
Hoban, P.4
Chilton-MacNeill, S.5
Campbell, C.E.6
Weksberg, R.7
Yeger, H.8
Reeve, A.E.9
Williams, B.R.G.10
-
8
-
-
0026457966
-
Inherited WT1 mutation in Denys-Drash syndrome
-
Coppes, M. J., Liefers, G. J., Higuchi, M., Zinn, A. B., Balfe, J. W., and Williams, B. R. G. (1992b). Inherited WT1 mutation in Denys-Drash syndrome. Cancer Res. 52: 6125-6128.
-
(1992)
Cancer Res.
, vol.52
, pp. 6125-6128
-
-
Coppes, M.J.1
Liefers, G.J.2
Higuchi, M.3
Zinn, A.B.4
Balfe, J.W.5
Williams, B.R.G.6
-
9
-
-
0028147486
-
The molecular genetics of Wilms tumor
-
Coppes, M. J., and Williams, B. R. G. (1994). The molecular genetics of Wilms tumor. Cancer Invest. 12: 57-65.
-
(1994)
Cancer Invest.
, vol.12
, pp. 57-65
-
-
Coppes, M.J.1
Williams, B.R.G.2
-
10
-
-
0025098654
-
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
-
Gessler, M., Poustka, A., Cavenee, W., Neve, R. L., Orkin, S. H., and Bruns, G. A. P. (1990). Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature 343: 774-778.
-
(1990)
Nature
, vol.343
, pp. 774-778
-
-
Gessler, M.1
Poustka, A.2
Cavenee, W.3
Neve, R.L.4
Orkin, S.H.5
Bruns, G.A.P.6
-
11
-
-
0028268123
-
Integration of physical, genetic and cytogenetic maps of human chromosome 7: Isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers
-
Green, E. D., Idol, J. R., Mohr-Tidwell, R. M., Braden, V. V., Peluso, D. C., Fulton, R. S., Massa, H. F., Magness, C. L., Wilson, A. M., Kimura, J., Weissenbach, J., and Trask, B. J. (1994). Integration of physical, genetic and cytogenetic maps of human chromosome 7: Isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Hum. Mol. Genet. 3: 489-501.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 489-501
-
-
Green, E.D.1
Idol, J.R.2
Mohr-Tidwell, R.M.3
Braden, V.V.4
Peluso, D.C.5
Fulton, R.S.6
Massa, H.F.7
Magness, C.L.8
Wilson, A.M.9
Kimura, J.10
Weissenbach, J.11
Trask, B.J.12
-
12
-
-
0028351728
-
Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome
-
Grundy, P. E., Telzerow, P. E., Breslow, N., Moksness, J., Huff, V., and Paterson, M. C. (1994). Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome. Cancer Res. 54: 2331-2333.
-
(1994)
Cancer Res.
, vol.54
, pp. 2331-2333
-
-
Grundy, P.E.1
Telzerow, P.E.2
Breslow, N.3
Moksness, J.4
Huff, V.5
Paterson, M.C.6
-
13
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-94 Généthon human genetic linkage map. Nature Genet. 7: 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
14
-
-
0024514494
-
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma
-
Henry, I., Grandjouan, S., Couillin, P., Barichard, F., Huerre-Jeanpierre, C., Glaser, T., Philip, T., Lenoir, G., Chaussain, J. L., and Junien, C. (1989). Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. Proc. Natl. Acad. Sci. USA 86: 3247-3251.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 3247-3251
-
-
Henry, I.1
Grandjouan, S.2
Couillin, P.3
Barichard, F.4
Huerre-Jeanpierre, C.5
Glaser, T.6
Philip, T.7
Lenoir, G.8
Chaussain, J.L.9
Junien, C.10
-
16
-
-
0026341035
-
Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors
-
Kaneko, Y., Homma, C., Maseki, N., Sakurai, M., and Hata, J.-i. (1991). Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res. 51: 5937-5942.
-
(1991)
Cancer Res.
, vol.51
, pp. 5937-5942
-
-
Kaneko, Y.1
Homma, C.2
Maseki, N.3
Sakurai, M.4
Hata, J.-I.5
-
17
-
-
0025911470
-
Chromosomal in situ suppression hybridization after Giemsa banding
-
Klever, M., Grond-Ginsbach, C., Scherthan, H., and Schroeder-kurth, T. M. (1991). Chromosomal in situ suppression hybridization after Giemsa banding. Hum. Genet. 86: 484-486.
-
(1991)
Hum. Genet.
, vol.86
, pp. 484-486
-
-
Klever, M.1
Grond-Ginsbach, C.2
Scherthan, H.3
Schroeder-Kurth, T.M.4
-
18
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5
-
Koufos, A., Grundy, P., Morgan, K., Aleck, K. A., Hadro, T., Lampkin, B. C., and Cavenee, W. K. (1989). Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am. J. Hum. Genet. 44: 711-719.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 711-719
-
-
Koufos, A.1
Grundy, P.2
Morgan, K.3
Aleck, K.A.4
Hadro, T.5
Lampkin, B.C.6
Cavenee, W.K.7
-
19
-
-
0024212964
-
Molecular nature of genetic changes resulting loss of heterozygosity of chromosome 11 in Wilms' tumours
-
Mannens, M., Slater, R. M., Heyting, C., Bliek, J., de Kraker, J., Coad, N., de Pagter-Holthuizen, P., and Pearson, P. L. (1988). Molecular nature of genetic changes resulting loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum. Genet. 81: 41-48.
-
(1988)
Hum. Genet.
, vol.81
, pp. 41-48
-
-
Mannens, M.1
Slater, R.M.2
Heyting, C.3
Bliek, J.4
De Kraker, J.5
Coad, N.6
De Pagter-Holthuizen, P.7
Pearson, P.L.8
-
20
-
-
0026691721
-
A third Wilms' tumor locus on chromosome 16q
-
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. (1992). A third Wilms' tumor locus on chromosome 16q. Cancer Res. 52: 3094-3098.
-
(1992)
Cancer Res.
, vol.52
, pp. 3094-3098
-
-
Maw, M.A.1
Grundy, P.E.2
Millow, L.J.3
Eccles, M.R.4
Dunn, R.S.5
Smith, P.J.6
Feinberg, A.P.7
Law, D.J.8
Paterson, M.C.9
Telzerow, P.E.10
Callen, D.F.11
Thompson, A.D.12
Richards, R.I.13
Reeve, A.E.14
-
21
-
-
0024995026
-
t(11;22) in three cases of peripheral neuroepithelioma
-
Miozzo, M., Sozzi, G., Calderone, C., Pilotti, S., Lombardi, L., Pierotti, M. A., and Della Porta, G. (1990). t(11;22) in three cases of peripheral neuroepithelioma. Genes Chromosomes Cancer 2: 163-165.
-
(1990)
Genes Chromosomes Cancer
, vol.2
, pp. 163-165
-
-
Miozzo, M.1
Sozzi, G.2
Calderone, C.3
Pilotti, S.4
Lombardi, L.5
Pierotti, M.A.6
Della Porta, G.7
-
22
-
-
0026339877
-
Report of the committee on chromosome changes in neoplasia. Human Gene Mapping 11
-
Mitelman, F., Kaneko, Y., and Trent, J. (1991). Report of the committee on chromosome changes in neoplasia. Human Gene Mapping 11. Cytogenet. Cell Genet. 58: 1053-1079.
-
(1991)
Cytogenet. Cell Genet.
, vol.58
, pp. 1053-1079
-
-
Mitelman, F.1
Kaneko, Y.2
Trent, J.3
-
23
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
-
Ogawa, O., Eccles, M. R., Szeto, J., McNoe, L. A., Yun, K., Maw, M. A., Smith, P. J., and Reeve, A. E. (1993a). Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 362: 749-751.
-
(1993)
Nature
, vol.362
, pp. 749-751
-
-
Ogawa, O.1
Eccles, M.R.2
Szeto, J.3
McNoe, L.A.4
Yun, K.5
Maw, M.A.6
Smith, P.J.7
Reeve, A.E.8
-
24
-
-
0027422302
-
Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism
-
Ogawa, O., Becroft, D. M., Morison, I. M., Eccles, M. R., Skeen, J. E., Mauger, D. C., and Reeve, A. E. (1993b). Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism. Nature Genet. 5: 408-412.
-
(1993)
Nature Genet.
, vol.5
, pp. 408-412
-
-
Ogawa, O.1
Becroft, D.M.2
Morison, I.M.3
Eccles, M.R.4
Skeen, J.E.5
Mauger, D.C.6
Reeve, A.E.7
-
25
-
-
0027379032
-
Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour
-
Park, S., Bernard, A., Bove, K. E., Sens, D. A., Hazen-Martin, D. J., Garvin, A. J., and Haber, D. A. (1993). Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour. Nature Genet. 5: 363-367.
-
(1993)
Nature Genet.
, vol.5
, pp. 363-367
-
-
Park, S.1
Bernard, A.2
Bove, K.E.3
Sens, D.A.4
Hazen-Martin, D.J.5
Garvin, A.J.6
Haber, D.A.7
-
26
-
-
0028840043
-
Involvement of chromosome 7 in Wilms tumor
-
Peier, A. M., Meloni, A. M., Erling, M. A., and Sandberg, A. A. (1995). Involvement of chromosome 7 in Wilms tumor. Cancer Genet. Cytogenet. 79: 92-94.
-
(1995)
Cancer Genet. Cytogenet.
, vol.79
, pp. 92-94
-
-
Peier, A.M.1
Meloni, A.M.2
Erling, M.A.3
Sandberg, A.A.4
-
27
-
-
0026094584
-
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier, J., Bruening, W., Kashtan, C. E., Mauer, S. M., Manivel, J. C., Striegel, J. E., Houghton, D. C., Junien, C., Habib, R., Fouser, L., Fine, R. N., Silverman, B. L., Haber, D. A., and Housman, D. (1991a). Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67: 437-447.
-
(1991)
Cell
, vol.67
, pp. 437-447
-
-
Pelletier, J.1
Bruening, W.2
Kashtan, C.E.3
Mauer, S.M.4
Manivel, J.C.5
Striegel, J.E.6
Houghton, D.C.7
Junien, C.8
Habib, R.9
Fouser, L.10
Fine, R.N.11
Silverman, B.L.12
Haber, D.A.13
Housman, D.14
-
28
-
-
0025788974
-
WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
-
Pelletier, J., Bruening, W., Li, F. P., Haber, D. A., Glaser, T., and Housman, D. E. (1991b). WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature 353: 431-434.
-
(1991)
Nature
, vol.353
, pp. 431-434
-
-
Pelletier, J.1
Bruening, W.2
Li, F.P.3
Haber, D.A.4
Glaser, T.5
Housman, D.E.6
-
29
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping, A. J., Reeve, A. E., Law, D. J., Young, M. R., Boehnke, M., and Feinberg, A. P. (1989). Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am. J. Hum. Genet. 44: 720-723.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 720-723
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Feinberg, A.P.6
-
30
-
-
0022446922
-
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
-
Pinkel, D., Straume, T., and Gray, J. W. (1986). Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc. Natl. Acad. Sci. USA 83: 2934-2938.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
31
-
-
0027295867
-
Homozygous intragenic loss of the WT1 locus in a sporadic intralobar Wilms' tumor
-
Radice, P., Pilotti, S., De Benedetti, V., Mondini, P., Miozzo, M., Luksch, R., Fossati-Bellani, F., Della Porta, G., and Pierotti, M. A. (1993). Homozygous intragenic loss of the WT1 locus in a sporadic intralobar Wilms' tumor. Int. J. Cancer 55: 174-176.
-
(1993)
Int. J. Cancer
, vol.55
, pp. 174-176
-
-
Radice, P.1
Pilotti, S.2
De Benedetti, V.3
Mondini, P.4
Miozzo, M.5
Luksch, R.6
Fossati-Bellani, F.7
Della Porta, G.8
Pierotti, M.A.9
-
32
-
-
0029078373
-
Allelotyping in Wilms tumors identifies a putative third tumor suppressor gene on chromosome 11
-
Radice, P., Perotti, D., De Benedetti, V., Mondini, P., Radice, M. T., Pilotti, S., Luksch, R., Fossati-Bellani, F., and Pierotti, M. A. (1995). Allelotyping in Wilms tumors identifies a putative third tumor suppressor gene on chromosome 11. Genomics 27: 497-501.
-
(1995)
Genomics
, vol.27
, pp. 497-501
-
-
Radice, P.1
Perotti, D.2
De Benedetti, V.3
Mondini, P.4
Radice, M.T.5
Pilotti, S.6
Luksch, R.7
Fossati-Bellani, F.8
Pierotti, M.A.9
-
33
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier, S., Johnson, L. A., Dobry, C. J., Ping, A. J., Grundy, P. E., and Feinberg, A. P. (1993). Relaxation of imprinted genes in human cancer. Nature 362: 747-749.
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
34
-
-
0024505754
-
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
-
Reeve, A. E., Sih, S. A., Raizis, A. M., and Feinberg, A. P. (1989). Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol. Cell. Biol. 9: 1799-1803.
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 1799-1803
-
-
Reeve, A.E.1
Sih, S.A.2
Raizis, A.M.3
Feinberg, A.P.4
-
35
-
-
0029011076
-
Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor
-
Rivera, H. (1995). Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor. Cancer Genet. Cytogenet. 81: 97-98.
-
(1995)
Cancer Genet. Cytogenet.
, vol.81
, pp. 97-98
-
-
Rivera, H.1
-
36
-
-
0027172255
-
Translocation (7;7)(p13;q21) in a Wilms' tumor
-
Sawyer, J. R., Winkel, E. W., Redman, J. F., and Roloson, G. J. (1993). Translocation (7;7)(p13;q21) in a Wilms' tumor. Cancer Genet. Cytogenet. 69: 57-59.
-
(1993)
Cancer Genet. Cytogenet.
, vol.69
, pp. 57-59
-
-
Sawyer, J.R.1
Winkel, E.W.2
Redman, J.F.3
Roloson, G.J.4
-
37
-
-
0026689597
-
Cytogenetics and molecular genetics of Wilms' tumor of childhood
-
Slater, R. M., and Mannens, M. M. A. M. (1992). Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet. Cytogenet. 61: 111-121.
-
(1992)
Cancer Genet. Cytogenet.
, vol.61
, pp. 111-121
-
-
Slater, R.M.1
Mannens, M.M.A.M.2
-
38
-
-
0029042877
-
Report of the second international workshop on human chromosome 7 mapping 1994
-
Tsui, L.-C., Donis-Keller, H., and Grzeschik, K-H. (1995). Report of the second international workshop on human chromosome 7 mapping 1994. Cytogenet. Cell Genet. 71: 2-21.
-
(1995)
Cytogenet. Cell Genet.
, vol.71
, pp. 2-21
-
-
Tsui, L.-C.1
Donis-Keller, H.2
Grzeschik, K.-H.3
-
39
-
-
0028298044
-
Fine structure analysis of the WT1 gene in sporadic Wilms tumors
-
Varanasi, R., Bardeesy, N., Ghahremani, M., Petruzzi, M.-J., Nowak, N., Adam, M. A., Grundy, P., Shows, T. B., and Pelletier, J. (1994). Fine structure analysis of the WT1 gene in sporadic Wilms tumors. Proc. Natl. Acad. Sci. USA 91: 3554-3558.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 3554-3558
-
-
Varanasi, R.1
Bardeesy, N.2
Ghahremani, M.3
Petruzzi, M.-J.4
Nowak, N.5
Adam, M.A.6
Grundy, P.7
Shows, T.B.8
Pelletier, J.9
-
40
-
-
0027131705
-
Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors
-
Waber, P. G., Chen, J., and Nisen, P. D. (1993). Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors. Cancer 72: 3732-3738.
-
(1993)
Cancer
, vol.72
, pp. 3732-3738
-
-
Waber, P.G.1
Chen, J.2
Nisen, P.D.3
-
41
-
-
0025346754
-
Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11
-
Wadey, R. B., Pal, N., Buckle, B., Yeomans, E., Pritchard, J., and Cowell, J. K. (1990). Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11. Oncogene 5: 901-907.
-
(1990)
Oncogene
, vol.5
, pp. 901-907
-
-
Wadey, R.B.1
Pal, N.2
Buckle, B.3
Yeomans, E.4
Pritchard, J.5
Cowell, J.K.6
-
42
-
-
0025318971
-
Chromosome analysis of 31 Wilms' tumors
-
Wang-Wuu, S., Soukup, S., Bove, K., Gotwals, B., and Lampkin, B. (1990). Chromosome analysis of 31 Wilms' tumors. Cancer Res. 50: 2786-2793.
-
(1990)
Cancer Res.
, vol.50
, pp. 2786-2793
-
-
Wang-Wuu, S.1
Soukup, S.2
Bove, K.3
Gotwals, B.4
Lampkin, B.5
-
43
-
-
0000739916
-
The use of PCR and ethidium bromide staining to detect length variation in short repeat units
-
Watkins, C., Warne, D., Kelsell, D., Beckmann, J., Nyberg, K., and Spurr, N. (1991). The use of PCR and ethidium bromide staining to detect length variation in short repeat units. Technique 3:175-178.
-
(1991)
Technique
, vol.3
, pp. 175-178
-
-
Watkins, C.1
Warne, D.2
Kelsell, D.3
Beckmann, J.4
Nyberg, K.5
Spurr, N.6
-
44
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg, R., Shen, D. R., Fei, Y. L., Song, Q. L., and Squire, J. (1993). Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nature Genet. 5: 143-150.
-
(1993)
Nature Genet.
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
45
-
-
0028032465
-
Germline and somatic abnormalities of chromosome 7 in Wilms' tumor
-
Wilmore, H. P., White, G. F. J., Howell, R. T., and Brown, K. W. (1994). Germline and somatic abnormalities of chromosome 7 in Wilms' tumor. Cancer Genet. Cytogenet. 77: 93-98.
-
(1994)
Cancer Genet. Cytogenet.
, vol.77
, pp. 93-98
-
-
Wilmore, H.P.1
White, G.F.J.2
Howell, R.T.3
Brown, K.W.4
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