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WT1 Mutation and 11P15 Loss of Heterozygosity Predict Relapse in Very Low-Risk Wilms Tumors Treated With Surgery Alone: A Children's Oncology Group Study

Journal of clinical oncology, 2011-02, Vol.29 (6), p.698-703

2011

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Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562

Clinical cancer research, 2009-10, Vol.15 (19), p.5985-5992

2009

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Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

American journal of medical genetics, 2004-06, Vol.127A (3), p.249-257

2004

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Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

The Journal of pediatrics, 1993-11, Vol.123 (5), p.673-678

1993

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Frequent association of β-catenin and WT1 mutations in Wilms tumors

Cancer research (Chicago, Ill.), 2000-11, Vol.60 (22), p.6288-6292

2000

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Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Oncogene, 2003-06, Vol.22 (24), p.3821-3826

2003

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Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Cancer research (Chicago, Ill.), 1994-05, Vol.54 (9), p.2331-2333

1994

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Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

Cancer research (Chicago, Ill.), 1998-04, Vol.58 (7), p.1387-1390

1998

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Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18

American journal of medical genetics, 2003-08, Vol.121A (1), p.52-55

2003

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Wilms tumor genetics

American journal of medical genetics, 1998-10, Vol.79 (4), p.260-267

Huff, Vicki

1998

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Lack of linkage of familial Wilms' tumour to chromosomal band 11p13

Nature (London), 1988-11, Vol.336 (6197), p.377-378

1988

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Nonlinkage of 16q markers to familial predisposition to wilms tumor

Cancer research (Chicago, Ill.), 1992-11, Vol.52 (21), p.6117-6120

1992

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Evidence for genetic heterogeneity in familial wilms' tumor

Cancer research (Chicago, Ill.), 1997-05, Vol.57 (10), p.1859-1862

1997

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RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology

JNCI : Journal of the National Cancer Institute, 1992-02, Vol.84 (3), p.181-187

1992

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Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.293-297

1991

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Parental origin of De Novo constitutional deletions of chromosomal band 11p13

American journal of human genetics, 1990-07, Vol.47 (1), p.155-160

1990

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WT1 Mutation and 11P15 Loss of Heterozygosity Predict Relapse in Very Low-Risk Wilms Tumors Treated With Surgery Alone: A Children's Oncology Group Study

Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562

Twenty-four new cases of WT1 germline mutations and review of the literature: Genotype/phenotype correlations for Wilms tumor development

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

Frequent association of β-catenin and WT1 mutations in Wilms tumors

Upregulation of c-MYC in WT1-mutant tumors: assessment of WT1 putative transcriptional targets using cDNA microarray expression profiling of genetically defined Wilms' tumors

Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome

Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors

Characterization of a Wilms tumor in a 9‐year‐old girl with trisomy 18

Wilms tumor genetics

Lack of linkage of familial Wilms' tumour to chromosomal band 11p13

Nonlinkage of 16q markers to familial predisposition to wilms tumor

Evidence for genetic heterogeneity in familial wilms' tumor

RNA Expression of the WT1 Gene in Wilms' Tumors in Relation to Histology

Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus

Parental origin of De Novo constitutional deletions of chromosomal band 11p13

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