Excess of multifocal tumors in nephroblastoma: implications for mechanisms of tumor development and genetic counseling

[1]  Md. Mohidul Hasan Genomic imprinting and carcinogenesis. , 1998, Histology and histopathology.

[2]  M. Skolnick,et al.  Familial predisposition to Wilms tumor does not segregate with the WT1 gene. , 1991, Genomics.

[3]  C. Sapienza,et al.  A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting , 1989 .

[4]  C. Junien,et al.  Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[5]  W. Cavenee,et al.  Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. , 1989, American journal of human genetics.

[6]  M. Surani,et al.  Genomic imprinting and embryonal tumours , 1989, Nature.

[7]  J. Williams,et al.  MATERNAL ALLELE LOSS IN WILMS' TUMOUR , 1989, The Lancet.

[8]  C. Heyting,et al.  Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours , 1988, Human Genetics.

[9]  L. Strong,et al.  Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13 , 1988, Nature.

[10]  W. Cavenee,et al.  Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11 , 1988, Nature.

[11]  B. Horsthemke,et al.  Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locus , 1987, Human Genetics.

[12]  L. Strong,et al.  Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. , 1987, American journal of human genetics.

[13]  W. Cavenee,et al.  Prediction of familial predisposition to retinoblastoma. , 1986, The New England journal of medicine.

[14]  Raymond L. White,et al.  Homozygosity of chromosome 13 in retinoblastoma. , 1984, The New England journal of medicine.

[15]  T. P. Dryja,et al.  Expression of recessive alleles by chromosomal mechanisms in retinoblastoma , 1983, Nature.

[16]  B. Gallie,et al.  Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma , 1983, Nature.

[17]  W. Benedict,et al.  Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D. , 1983, Science.

[18]  N. Breslow,et al.  Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study. , 1982, Journal of the National Cancer Institute.

[19]  A. Knudson,et al.  Mutation and cancer: a model for Wilms' tumor of the kidney. , 1972, Journal of the National Cancer Institute.

[20]  A. Knudson Mutation and cancer: statistical study of retinoblastoma. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[21]  E. Matsunaga,et al.  Genetics of Wilms' tumor , 2004, Human Genetics.

[22]  A. Feinberg,et al.  Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. , 1989, American journal of human genetics.

[23]  C. Sapienza,et al.  A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[24]  R. Fisher,et al.  On the Mathematical Foundations of Theoretical Statistics , 1922 .