-
1
-
-
0026094584
-
Germline mutations in the Wilms tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier J, Bruening W, Kashtan CE, et al. Germline mutations in the Wilms tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 1991;67:437-447.
-
(1991)
Cell
, vol.67
, pp. 437-447
-
-
Pelletier, J.1
Bruening, W.2
Kashtan, C.E.3
-
2
-
-
0030891372
-
A clinical overview of WT1 gene mutations
-
Little M, Wells C. A clinical overview of WT1 gene mutations. Hum Mutat 1997;9:209-225.
-
(1997)
Hum Mutat
, vol.9
, pp. 209-225
-
-
Little, M.1
Wells, C.2
-
3
-
-
13044266382
-
A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome
-
Patek CE, Little MH, Fleming S, et al. A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome. Proc Natl Acad Sci USA 1999;96:2931-2936.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2931-2936
-
-
Patek, C.E.1
Little, M.H.2
Fleming, S.3
-
4
-
-
16944365351
-
Donor splice-site mutations in WT1 are responsible for Frasier syndrome
-
Barbaux S, Niaudet P, Gubler MC, et al. Donor splice-site mutations in WT1 are responsible for Frasier syndrome. Nat Genet 1997;17:467-470.
-
(1997)
Nat Genet
, vol.17
, pp. 467-470
-
-
Barbaux, S.1
Niaudet, P.2
Gubler, M.C.3
-
5
-
-
0031922880
-
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/- KTS splice isoforms
-
Klamt B, Koziell A, Poulat F, et al. Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/- KTS splice isoforms. Hum Mol Genet 1998;7:709-714.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 709-714
-
-
Klamt, B.1
Koziell, A.2
Poulat, F.3
-
6
-
-
0014119131
-
Association d'un syndrome anatomopathologique de pseudohermaphrodisme masculin, d'une tumeur de Wilms, d'une néphropathie parenchymateuse et d'un mosaicisme.
-
Denys P, Malvaux P, Van Den Berghe H, et al. Association d'un syndrome anatomopathologique de pseudohermaphrodisme masculin, d'une tumeur de Wilms, d'une néphropathie parenchymateuse et d'un mosaicisme. Arch Fr Pediatr 1967;24:729-739.
-
(1967)
Arch Fr Pediatr
, vol.24
, pp. 729-739
-
-
Denys, P.1
Malvaux, P.2
Van Den Berghe, H.3
-
7
-
-
0014775569
-
A syndrome of pseudohermaphroditism, Wilms tumor, hypertension, and degenerative renal disease
-
Drash A, Sherman F, Hartmann WH, Blizzard RM. A syndrome of pseudohermaphroditism, Wilms tumor, hypertension, and degenerative renal disease. J Pediatr 1970;76:585-593.
-
(1970)
J Pediatr
, vol.76
, pp. 585-593
-
-
Drash, A.1
Sherman, F.2
Hartmann, W.H.3
Blizzard, R.M.4
-
8
-
-
0000786264
-
Gonadoblastoma associated with pure gonadal dysgenesis in monozygous twins
-
Frasier SD, Bashore RA, Mosier HD. Gonadoblastoma associated with pure gonadal dysgenesis in monozygous twins. J Pediatr 1964;64:740-745.
-
(1964)
J Pediatr
, vol.64
, pp. 740-745
-
-
Frasier, S.D.1
Bashore, R.A.2
Mosier, H.D.3
-
9
-
-
0032913826
-
The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms tumor
-
Barbosa AS, Hadjiathanasiou CG, Theodoridis C, et al. The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms tumor. Hum Mutat 1999;13:146-153.
-
(1999)
Hum Mutat
, vol.13
, pp. 146-153
-
-
Barbosa, A.S.1
Hadjiathanasiou, C.G.2
Theodoridis, C.3
-
10
-
-
17344364993
-
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
-
Jeanpierre C, Denamur E, Henry I, et al. Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database. Am J Hum Genet 1998;62:824-833.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 824-833
-
-
Jeanpierre, C.1
Denamur, E.2
Henry, I.3
-
11
-
-
0036157514
-
Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood
-
Vujanic GM, Sandstedt B, Harms D, et al. Revised International Society of Paediatric Oncology (SIOP) working classification of renal tumors of childhood. Med Pediatr Oncol 2002;38:79-82.
-
(2002)
Med Pediatr Oncol
, vol.38
, pp. 79-82
-
-
Vujanic, G.M.1
Sandstedt, B.2
Harms, D.3
-
12
-
-
33748422544
-
-
Houk CP, Hughes IA, Ahmed SF, et al. Writing Committee for the International Intersex Consensus Conference Participants. Summary of consensus statement on intersex disorders and their management. Pediatrics 2006;118:753-757.
-
Houk CP, Hughes IA, Ahmed SF, et al. Writing Committee for the International Intersex Consensus Conference Participants. Summary of consensus statement on intersex disorders and their management. Pediatrics 2006;118:753-757.
-
-
-
-
13
-
-
0000537977
-
-
editors. Principles and practice of pediatric oncology. Philadelphia: JB Lippincott-Raven;
-
Green DM, Coppes MJ, Breslow NE, et al. Wilms tumor. In: Pizzo PA, Poplack DG, editors. Principles and practice of pediatric oncology. Philadelphia: JB Lippincott-Raven; 1997. pp. 733-759.
-
(1997)
Wilms tumor
, pp. 733-759
-
-
Green, D.M.1
Coppes, M.J.2
Breslow, N.E.3
-
14
-
-
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, et al. 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 1997;94:3972-3977.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 3972-3977
-
-
Schumacher, V.1
Schneider, S.2
Figge, A.3
-
15
-
-
0031611708
-
Loss of WT1 function leads to ectopic myogenesis in Wilms tumour
-
Miyagawa K, Kent J, Moore A, et al. Loss of WT1 function leads to ectopic myogenesis in Wilms tumour. Nat Genet 1998;18:15-17.
-
(1998)
Nat Genet
, vol.18
, pp. 15-17
-
-
Miyagawa, K.1
Kent, J.2
Moore, A.3
-
16
-
-
0027379032
-
Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms tumour
-
Park S, Bernard A, Bove KE, et al. Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms tumour. Nat Genet 1993;5:363-367.
-
(1993)
Nat Genet
, vol.5
, pp. 363-367
-
-
Park, S.1
Bernard, A.2
Bove, K.E.3
-
17
-
-
0025821233
-
Nephrogenic rests in Wilms tumor patients with the Drash syndrome
-
Heppe RK, Koyle MA, Beckwith JB. Nephrogenic rests in Wilms tumor patients with the Drash syndrome. J Urol 1991;145:1225-1228.
-
(1991)
J Urol
, vol.145
, pp. 1225-1228
-
-
Heppe, R.K.1
Koyle, M.A.2
Beckwith, J.B.3
-
18
-
-
0035943454
-
Life, sex, and WT1 isoforms - Three amino acids can make all the difference
-
Hastie ND. Life, sex, and WT1 isoforms - Three amino acids can make all the difference. Cell 2001;106:391-394.
-
(2001)
Cell
, vol.106
, pp. 391-394
-
-
Hastie, N.D.1
-
19
-
-
7044262957
-
Frequency and heritability of WT1 mutations in nonsyndromic Wilms tumor patients: AUK Children's Cancer Study Group Study
-
Little SE, Hanks SP, King-Underwood L, et al. Frequency and heritability of WT1 mutations in nonsyndromic Wilms tumor patients: AUK Children's Cancer Study Group Study. J Clin Oncol 2004;22:4140-4146.
-
(2004)
J Clin Oncol
, vol.22
, pp. 4140-4146
-
-
Little, S.E.1
Hanks, S.P.2
King-Underwood, L.3
-
20
-
-
0028196679
-
Infrequent mutation of the WT1 gene in 77 Wilms Tumors
-
Gessler M, König A, Arden K, et al. Infrequent mutation of the WT1 gene in 77 Wilms Tumors. Hum Mutat 1994;3:212-222.
-
(1994)
Hum Mutat
, vol.3
, pp. 212-222
-
-
Gessler, M.1
König, A.2
Arden, K.3
-
21
-
-
0022357227
-
The nephropathy associated with male pseudohermaphroditism and Wilms tumor (Drash syndrome): A distinctive glomerular lesion-report of 10 cases
-
Habib R, Loirat C, Gubler MC, et al. The nephropathy associated with male pseudohermaphroditism and Wilms tumor (Drash syndrome): A distinctive glomerular lesion-report of 10 cases. Clin Nephrol 1985;24:269-278.
-
(1985)
Clin Nephrol
, vol.24
, pp. 269-278
-
-
Habib, R.1
Loirat, C.2
Gubler, M.C.3
|