-
1
-
-
0029765587
-
Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization
-
Altura RA, Valentine M, Li H, Boyett JM, Shearer P, Grundy P, Shapiro DN, Look AT (1996) Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization. Cancer Res 56:3837-3841.
-
(1996)
Cancer Res
, vol.56
, pp. 3837-3841
-
-
Altura, R.A.1
Valentine, M.2
Li, H.3
Boyett, J.M.4
Shearer, P.5
Grundy, P.6
Shapiro, D.N.7
Look, A.T.8
-
2
-
-
0028839369
-
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis
-
Austruy E, Candon S, Henry I, Gyapay G, Tournade MF, Mannens M, Gallen D, Junien C, Jeanpierre C (1995) Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis. Genes Chromosomes Cancer 14:285-294.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 285-294
-
-
Austruy, E.1
Candon, S.2
Henry, I.3
Gyapay, G.4
Tournade, M.F.5
Mannens, M.6
Gallen, D.7
Junien, C.8
Jeanpierre, C.9
-
3
-
-
0004270170
-
-
New York: John Wiley & Sons, Inc.
-
Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K (1994) Current Protocols in Molecular Biology. New York: John Wiley & Sons, Inc.
-
(1994)
Current Protocols in Molecular Biology
-
-
Ausubel, F.M.1
Brent, R.2
Kingston, R.E.3
Moore, D.D.4
Seidman, J.G.5
Smith, J.A.6
Struhl, K.7
-
4
-
-
0028168146
-
Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbors p53 gene mutations
-
Bardeesy N, Falkoff D, Petruzzi MJ, Nowak N, Zabel B, Adam M, Aguiar MC, Grundy P, Shows T, Pelletier J (1994) Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbors p53 gene mutations. Nat Genet 7:91-97.
-
(1994)
Nat Genet
, vol.7
, pp. 91-97
-
-
Bardeesy, N.1
Falkoff, D.2
Petruzzi, M.J.3
Nowak, N.4
Zabel, B.5
Adam, M.6
Aguiar, M.C.7
Grundy, P.8
Shows, T.9
Pelletier, J.10
-
5
-
-
0028892269
-
Single nucleotide polymorphisms in the human E-cadherin gene
-
Becker KK, Reich U, Schott C, Hofler H (1995) Single nucleotide polymorphisms in the human E-cadherin gene. Hum Genet 96:739-740.
-
(1995)
Hum Genet
, vol.96
, pp. 739-740
-
-
Becker, K.K.1
Reich, U.2
Schott, C.3
Hofler, H.4
-
6
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Krai A, Yeger H, Lewis WH, Jones C, Housman DE (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
Krai, A.8
Yeger, H.9
Lewis, W.H.10
Jones, C.11
Housman, D.E.12
-
7
-
-
0026685962
-
Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of 3 distinct regions and a limited role for nondisjunction or mitotic recombination
-
Coppes MJ, Bonetta L, Huang A, Huban P, Chiltonmacneill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BRG (1992) Loss of heterozygosity mapping in Wilms' tumor indicates the involvement of 3 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
Huban, P.4
Chiltonmacneill, S.5
Campbell, C.E.6
Weksberg, R.7
Yeger, H.8
Reeve, A.E.9
Brg, W.10
-
8
-
-
0030069636
-
The new SIOP (Stockholm) working classification of renal tumours of childhood. International Society of Paediatric Oncology (letter)
-
Delemarre JF, Sandstedt B, Harms D, Boccon-Gibod L, Vujanic GM (1996) The new SIOP (Stockholm) working classification of renal tumours of childhood. International Society of Paediatric Oncology (letter). Med Pediatr Oncol 26:145-146.
-
(1996)
Med Pediatr Oncol
, vol.26
, pp. 145-146
-
-
Delemarre, J.F.1
Sandstedt, B.2
Harms, D.3
Boccon-Gibod, L.4
Vujanic, G.M.5
-
9
-
-
0029653645
-
An integrated physical map of human chromosome 16
-
Doggett NA, Goodwin LA, Tesmer JG, Meincke LJ, Brnce DC, Clark LM, Altherr MR, Ford AA, Chi HC, Marrone BL, Longmire JL, Lane SA, Whitmore SA, Lowenstein MG, Sutherland RD, Mundt MO, Knill EH, Bruno WJ, Macken CA, Torney DC, Wu JR, Griffith J, Sutherland GR, Deaven LL, Callen DF (1995) An integrated physical map of human chromosome 16. Nature 377:335-365.
-
(1995)
Nature
, vol.377
, pp. 335-365
-
-
Doggett, N.A.1
Goodwin, L.A.2
Tesmer, J.G.3
Meincke, L.J.4
Brnce, D.C.5
Clark, L.M.6
Altherr, M.R.7
Ford, A.A.8
Chi, H.C.9
Marrone, B.L.10
Longmire, J.L.11
Lane, S.A.12
Whitmore, S.A.13
Lowenstein, M.G.14
Sutherland, R.D.15
Mundt, M.O.16
Knill, E.H.17
Bruno, W.J.18
Macken, C.A.19
Torney, D.C.20
Wu, J.R.21
Griffith, J.22
Sutherland, G.R.23
Deaven, L.L.24
Callen, D.F.25
more..
-
10
-
-
0027459389
-
The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney
-
Garvin AJ, Re GG, Tarnowski BI, Hazenmartin DJ, Sens DA (1993) The G401 cell line, utilized for studies of chromosomal changes in Wilms' tumor, is derived from a rhabdoid tumor of the kidney. Am J Pathol 142:375-380.
-
(1993)
Am J Pathol
, vol.142
, pp. 375-380
-
-
Garvin, A.J.1
Re, G.G.2
Tarnowski, B.I.3
Hazenmartin, D.J.4
Sens, D.A.5
-
11
-
-
0025098654
-
Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping
-
Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GA (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.6
-
12
-
-
0028196679
-
Infrequent mutation of the WT1 gene in 77 Wilms' tumors
-
Gessler M, König A, Arden K, Grundy P, Orkin S, Sallan S, Peters C, Ruyle S, Mandell J, Li F, Cavenee W, Bruns G (1994) Infrequent mutation of the WT1 gene in 77 Wilms' tumors. Hum Mut 3:212-222.
-
(1994)
Hum Mut
, vol.3
, pp. 212-222
-
-
Gessler, M.1
König, A.2
Arden, K.3
Grundy, P.4
Orkin, S.5
Sallan, S.6
Peters, C.7
Ruyle, S.8
Mandell, J.9
Li, F.10
Cavenee, W.11
Bruns, G.12
-
13
-
-
0023683531
-
Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
-
Grundy P, Koufos A, Morgan K, Li KP, Meadows AT, Cavenee WK (1988) Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 366:374-376.
-
(1988)
Nature
, vol.366
, pp. 374-376
-
-
Grundy, P.1
Koufos, A.2
Morgan, K.3
Li, K.P.4
Meadows, A.T.5
Cavenee, W.K.6
-
14
-
-
0028351728
-
Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome
-
Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC (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
-
15
-
-
0029838115
-
Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: A preliminary analysis
-
Grundy P, Telzerow P, Moksness J, Breslow NE (1996) Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: A preliminary analysis. Med Pediatr Oncol 27:429-433.
-
(1996)
Med Pediatr Oncol
, vol.27
, pp. 429-433
-
-
Grundy, P.1
Telzerow, P.2
Moksness, J.3
Breslow, N.E.4
-
16
-
-
0028829767
-
Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer
-
Hoggard N, Hey Y, Brintnell B, James L, Jones D, Mitchell E, Weissenbach J, Varley JM (1995) Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer. Genomics 30:233-243.
-
(1995)
Genomics
, vol.30
, pp. 233-243
-
-
Hoggard, N.1
Hey, Y.2
Brintnell, B.3
James, L.4
Jones, D.5
Mitchell, E.6
Weissenbach, J.7
Varley, J.M.8
-
17
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers JMN, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillonmiller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP (1995) Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci USA 92:12456-12460.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillonmiller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannens, M.19
Feinberg, A.P.20
more..
-
19
-
-
0026457965
-
Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
-
Huff V, Reeve AE, Leppert M, Strong LC, Douglass EC, Geiser CF, Li KP, Meadows A, Callen DF, Lenoir G, Saunders GF (1992) Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Cancer Res 52:6117-6120.
-
(1992)
Cancer Res
, vol.52
, pp. 6117-6120
-
-
Huff, V.1
Reeve, A.E.2
Leppert, M.3
Strong, L.C.4
Douglass, E.C.5
Geiser, C.F.6
Li, K.P.7
Meadows, A.8
Callen, D.F.9
Lenoir, G.10
Saunders, G.F.11
-
20
-
-
0030940740
-
Evidence for genetic heterogeneity in familial VVilms' tumor
-
Huff V, Amos CI, Douglass EC, Fisher R, Geiser CF, Krill CE, Li FP, Strong LC, McDonald JM (1997) Evidence for genetic heterogeneity in familial VVilms' tumor. Cancer Res 57:1859-1862.
-
(1997)
Cancer Res
, vol.57
, pp. 1859-1862
-
-
Huff, V.1
Amos, C.I.2
Douglass, E.C.3
Fisher, R.4
Geiser, C.F.5
Krill, C.E.6
Li, F.P.7
Strong, L.C.8
McDonald, J.M.9
-
21
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms' tumor locus both map to 11p15.5
-
Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK (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
Kalbakji, A.7
Cavenee, W.K.8
-
22
-
-
0029864908
-
Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome
-
Lahoti C, Thorner P, Malkin ID, Yeger H (1996) Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome. Am J Pathol 148:1577-1589.
-
(1996)
Am J Pathol
, vol.148
, pp. 1577-1589
-
-
Lahoti, C.1
Thorner, P.2
Malkin, I.D.3
Yeger, H.4
-
23
-
-
0031214256
-
Allelic imbalance at chromosome 1q21 in Wilms' tumor
-
Law MH, Algar E, Little M (1997) Allelic imbalance at chromosome 1q21 in Wilms' tumor. Cancer Genet Cytogenet 97:54-59.
-
(1997)
Cancer Genet Cytogenet
, vol.97
, pp. 54-59
-
-
Law, M.H.1
Algar, E.2
Little, M.3
-
24
-
-
0030610261
-
Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome
-
Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP (1997) Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome. Am J Hum Genet 61:304-309.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 304-309
-
-
Lee, M.P.1
Debaun, M.2
Randhawa, G.3
Reichard, B.A.4
Elledge, S.J.5
Feinberg, A.P.6
-
25
-
-
0030891372
-
A clinical overview of WT1 gene mutations
-
Little M, Wells C (1997) A clinical overview of WT1 gene mutations. Hum Mutat 9:209-225.
-
(1997)
Hum Mutat
, vol.9
, pp. 209-225
-
-
Little, M.1
Wells, C.2
-
26
-
-
0024212964
-
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumors
-
Mannens M, Slater RM, Heyting C, Blick J, de Kraker J, Coud N, de Paper-Holthuizen P, Pearson PL (1988) Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumors. Hum Genet 81:41-48.
-
(1988)
Hum Genet
, vol.81
, pp. 41-48
-
-
Mannens, M.1
Slater, R.M.2
Heyting, C.3
Blick, J.4
De Kraker, J.5
Coud, N.6
De Paper-Holthuizen, P.7
Pearson, P.L.8
-
27
-
-
0026691721
-
A third Wilms' tumor locus on chromosome 16q
-
Maw MA, Grundy PK, Millow LJ, Eccles MR, Dunn RS, Smith PJ, Feinberg AP, Law DJ, Paterson MC, Telzerow PE, Callen DF, Thompson AD, Richards RI, Reeve AE (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.K.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
-
28
-
-
0030297969
-
Mapping of a putative tumor suppressor locus to proximal 7p in Wilms' tumors
-
Miozzo M, Perotti D, Minoletti F, Mondini P, Pilotti S, Luksch R, Fossati-Bellani F, Picrotti MA, Sozzi G, Radice P (1996) Mapping of a putative tumor suppressor locus to proximal 7p in Wilms' tumors. Genomics 37:310-315.
-
(1996)
Genomics
, vol.37
, pp. 310-315
-
-
Miozzo, M.1
Perotti, D.2
Minoletti, F.3
Mondini, P.4
Pilotti, S.5
Luksch, R.6
Fossati-Bellani, F.7
Picrotti, M.A.8
Sozzi, G.9
Radice, P.10
-
29
-
-
0030610260
-
Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors
-
O'Keefe 13, Dao D, Zhao L, Sanderson R, Warburton D, Weiss L, Anyane-Yeboa K, Tycko B (1997) Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors. Am J Hum Genet 61:295-303.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 295-303
-
-
O'Keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Weiss, L.6
Anyane-Yeboa, K.7
Tycko, B.8
-
30
-
-
0029078373
-
Allelotyping in Wilms' tumors identifies a putative third tumor suppressor gene on chromosome 11
-
Radice P, Perotti D, Debenedetti V, Mondini P, Radice MT, Pilotti S, Luksch R, Bellani FE, Pierotti MA (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
Debenedetti, V.3
Mondini, P.4
Radice, M.T.5
Pilotti, S.6
Luksch, R.7
Bellani, F.E.8
Ma, P.9
-
31
-
-
0030017174
-
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21
-
Rahman N, Arbour L, Tonin P, Renshaw J, Pelletier J, Baruchel S, Pritchard-Jones K, Stratton MR, Narod SA (1996) Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21. Nat Genet 13:461-463.
-
(1996)
Nat Genet
, vol.13
, pp. 461-463
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Renshaw, J.4
Pelletier, J.5
Baruchel, S.6
Pritchard-Jones, K.7
Stratton, M.R.8
Narod, S.A.9
-
32
-
-
0024505754
-
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
-
Reeve AE, Sih SA, Raizis AM, Feinberg AP (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
-
33
-
-
0031214796
-
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/wt2 region
-
Reid LH, Davies C, Cooper PR, Crider-Miller SJ, Sait SN, Nowak NJ, Evans G, Stanbridge EJ, deJong P, Shows TB, Weissman BE, Higgins MJ (1997) A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/wt2 region. Genomics 43:366-375.
-
(1997)
Genomics
, vol.43
, pp. 366-375
-
-
Reid, L.H.1
Davies, C.2
Cooper, P.R.3
Crider-Miller, S.J.4
Sait, S.N.5
Nowak, N.J.6
Evans, G.7
Stanbridge, E.J.8
DeJong, P.9
Shows, T.B.10
Weissman, B.E.11
Higgins, M.J.12
-
34
-
-
0030032087
-
Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors
-
Schofield DE, Beckwith JB, Sklar J (1996) Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors. Genes Chromosomes Cancer 15:10-17.
-
(1996)
Genes Chromosomes Cancer
, vol.15
, pp. 10-17
-
-
Schofield, D.E.1
Beckwith, J.B.2
Sklar, J.3
-
35
-
-
0030889197
-
Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms' tumors of stromal-predominant histology
-
Schumacher V, Schneider S, Figge A, Wildhardt G, Harms D, Schmidt D, Weirich A, Ludwig R, Royer-Pokora B (1997) Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms' tumors of stromal-predominant histology. Proc Natl Acad Sci USA 94:3972-3977.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3972-3977
-
-
Schumacher, V.1
Schneider, S.2
Figge, A.3
Wildhardt, G.4
Harms, D.5
Schmidt, D.6
Weirich, A.7
Ludwig, R.8
Royer-Pokora, B.9
-
36
-
-
0030841547
-
Comparative genomic hybridization analysis of Wilms' tumors
-
Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voute PA, Westerveld A, Slater R, Mannens M (1997) (Comparative genomic hybridization analysis of Wilms' tumors. Cytogenet Cell Genet 77:296-303.
-
(1997)
Cytogenet Cell Genet
, vol.77
, pp. 296-303
-
-
Steenman, M.1
Redeker, B.2
De Meulemeester, M.3
Wiesmeijer, K.4
Voute, P.A.5
Westerveld, A.6
Slater, R.7
Mannens, M.8
-
37
-
-
0028935017
-
Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor
-
Taniguchi T, Sullivan MJ, Ogawa O, Reeve AE (1995) Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms' tumor. Proc Natl Acad Sci USA 92:2159-2163.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2159-2163
-
-
Taniguchi, T.1
Sullivan, M.J.2
Ogawa, O.3
Reeve, A.E.4
-
38
-
-
0028298044
-
Fine structure analysis of the WT1 gene in sporadic Wilms' tumors
-
Varanasi R, Bardeesy N, Ghahremani M, Petruzzi MJ, Nowak N, Adam MA, Grundy P, Shows TB, 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
-
39
-
-
0030333738
-
Report of the second international workshop on human chromosome 1 mapping 1995
-
Weith A, Brodeur GM, Bruns GA, Matise TC, Mischke D, Nizetic D, Seidin MF, van Roy N, Vance J (1996) Report of the second international workshop on human chromosome 1 mapping 1995. Cytogenet Cell Genet 72:114-144.
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 114-144
-
-
Weith, A.1
Brodeur, G.M.2
Bruns, G.A.3
Matise, T.C.4
Mischke, D.5
Nizetic, D.6
Seidin, M.F.7
Van Roy, N.8
Vance, J.9
-
40
-
-
0029055009
-
Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis
-
Winqvist R, Hampton GM, Mannermaa A, Blanco G, Alavaikko M, Kiviniemi H, Taskinen PJ, Kvans GA, Wright FA, Newsham I, Cavenee WK (1995) Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis. Cancer Res 55:2660-2664.
-
(1995)
Cancer Res
, vol.55
, pp. 2660-2664
-
-
Winqvist, R.1
Hampton, G.M.2
Mannermaa, A.3
Blanco, G.4
Alavaikko, M.5
Kiviniemi, H.6
Taskinen, P.J.7
Kvans, G.A.8
Wright, F.A.9
Newsham, I.10
Cavenee, W.K.11
|