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