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Pax-2 is a DNA-Binding Protein Expressed in Embryonic Kidney and Wilms Tumor

Proceedings of the National Academy of Sciences - PNAS, 1992-02, Vol.89 (4), p.1179-1183

1992

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There is no role for hyperfractionated radiotherapy in the management of children with newly diagnosed diffuse intrinsic brainstem tumors: results of a pediatric oncology group phase III trial comparing conventional vs. hyperfractionated radiotherapy

International journal of radiation oncology, biology, physics, 1999-03, Vol.43 (5), p.959-964

1999

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Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study

Journal of clinical oncology, 1991-04, Vol.9 (4), p.581-591

1991

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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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Detection of the (11;22)(q24;q12) translocation of Ewing's sarcoma and peripheral neuroectodermal tumor by reverse transcription polymerase chain reaction

The American journal of pathology, 1993-11, Vol.143 (5), p.1294-1300

1993

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Medulloblastoma in very young children: outcome of definitive craniospinal irradiation following incomplete response to chemotherapy

Journal of clinical oncology, 1994-06, Vol.12 (6), p.1212-1216

1994

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Amplification of the gli gene in childhood sarcomas

Cancer research (Chicago, Ill.), 1989-10, Vol.49 (19), p.5407-5413

1989

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Myeloperoxidase promotor polymorphism and risk of hepatoblastoma

International journal of cancer, 2003-08, Vol.106 (2), p.205-207

2003

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Splice-site mutation of the p53 gene in a family with hereditary breast-ovarian cancer

Oncogene, 1994, Vol.9 (1), p.97-102

1994

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Solid alveolar rhabdomyosarcomas with the t(2;13). Report of two cases with diagnostic implications

The American journal of surgical pathology, 1994-05, Vol.18 (5), p.474-478

1994

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Unique expression of the human Evi-1 gene in an endometrial carcinoma cell line: sequence of cDNAs and structure of alternatively spliced transcripts

Oncogene, 1990-07, Vol.5 (7), p.963-971

1990

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Chromosome translocation in peripheral neuroepithelioma

The New England journal of medicine, 1984-08, Vol.311 (9), p.584-585

1984

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Preirradiation cisplatin and etoposide in the treatment of high-risk medulloblastoma and other malignant embryonal tumors of the central nervous system: a phase II study

Journal of clinical oncology, 1990-02, Vol.8 (2), p.330-336

1990

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Chemotherapy can convert unresectable hepatoblastoma

Journal of pediatric surgery, 1992-08, Vol.27 (8), p.1080-1084

1992

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CCND1 polymorphism and age of onset of hepatoblastoma

Oncogene, 2004-06, Vol.23 (27), p.4789-4792

2004

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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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A specific chromosomal abnormality in rhabdomyosarcoma

Cytogenetic and genome research, 1987-01, Vol.45 (3-4), p.148-155

1987

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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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Oncogene amplification in pediatric brain tumors

Cancer research (Chicago, Ill.), 1990-05, Vol.50 (10), p.2987-2990

1990

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Bilateral Wilms tumor. Review of outcome, associated abnormalities, and late effects in 36 pediatric patients treated at a single institution

Cancer, 1993-08, Vol.72 (4), p.1422-1426

1993

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An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

Cell, 1990-06, Vol.61 (7), p.1257-1269

1990

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Relation of tumor-cell ploidy to survival in children with medulloblastoma

Journal of clinical oncology, 1993-11, Vol.11 (11), p.2211-2217

1993

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Relationship of tumor-cell ploidy to histologic subtype and treatment outcome in children and adolescents with unresectable rhabdomyosarcoma

Journal of clinical oncology, 1991-01, Vol.9 (1), p.159-166

1991

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Hyperdiploidy and chromosomal rearrangements define the anaplastic variant of Wilms' tumor

Journal of clinical oncology, 1986-06, Vol.4 (6), p.975-981

1986

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Chromosome 1 Abnormalities: A Common Feature of Pediatric Solid Tumors

JNCI : Journal of the National Cancer Institute, 1985-07, Vol.75 (1), p.51-54

1985

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Pax-2 is a DNA-Binding Protein Expressed in Embryonic Kidney and Wilms Tumor

There is no role for hyperfractionated radiotherapy in the management of children with newly diagnosed diffuse intrinsic brainstem tumors: results of a pediatric oncology group phase III trial comparing conventional vs. hyperfractionated radiotherapy

Clinical relevance of tumor cell ploidy and N-myc gene amplification in childhood neuroblastoma: a Pediatric Oncology Group study

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

Detection of the (11;22)(q24;q12) translocation of Ewing's sarcoma and peripheral neuroectodermal tumor by reverse transcription polymerase chain reaction

Medulloblastoma in very young children: outcome of definitive craniospinal irradiation following incomplete response to chemotherapy

Amplification of the gli gene in childhood sarcomas

Myeloperoxidase promotor polymorphism and risk of hepatoblastoma

Splice-site mutation of the p53 gene in a family with hereditary breast-ovarian cancer

Solid alveolar rhabdomyosarcomas with the t(2;13). Report of two cases with diagnostic implications

Unique expression of the human Evi-1 gene in an endometrial carcinoma cell line: sequence of cDNAs and structure of alternatively spliced transcripts

Chromosome translocation in peripheral neuroepithelioma

Preirradiation cisplatin and etoposide in the treatment of high-risk medulloblastoma and other malignant embryonal tumors of the central nervous system: a phase II study

Chemotherapy can convert unresectable hepatoblastoma

CCND1 polymorphism and age of onset of hepatoblastoma

Evidence for genetic heterogeneity in familial wilms' tumor

A specific chromosomal abnormality in rhabdomyosarcoma

Nonlinkage of 16q markers to familial predisposition to wilms tumor

Oncogene amplification in pediatric brain tumors

Bilateral Wilms tumor. Review of outcome, associated abnormalities, and late effects in 36 pediatric patients treated at a single institution

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

Relation of tumor-cell ploidy to survival in children with medulloblastoma

Relationship of tumor-cell ploidy to histologic subtype and treatment outcome in children and adolescents with unresectable rhabdomyosarcoma

Hyperdiploidy and chromosomal rearrangements define the anaplastic variant of Wilms' tumor

Chromosome 1 Abnormalities: A Common Feature of Pediatric Solid Tumors

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