Aniridia, Wilms' tumor and human chromosome 11

References

• Alvarado C. S., Verras A., Ragab A. H. Hilateral Wilms' tumor. Wilms' Tumor: Clinical and Biological Manifestations, C. Pocheldy, E. S. Baum. Elsevier. 1984; 89–102
   Google Scholar
• Avner P., Amar L., Dandolo L., Guenet J. L. Genetic analysis of the mouse using interspecific crosses. Trends in Gener. 1988; 4: 18–23
   PubMedGoogle Scholar
• Harlow D. P., Lehrach H. Genetics by gel electrophoresis; the impact of pulsed field gel electrophoresis on mammalian genetics. Trends in Genet. 1987; 3: 167–171
   Google Scholar
• Berg J. M. Potential metal‐binding domains in nucleic acid binding proteins. Science 1986; 232: 485
   PubMed Web of Science ®Google Scholar
• Bickmore W. A., et al. Hitch‐hiking from Hrasl to the WAGR locus with CMGT markers. Nucl. Acids Res. 1988; 16: 51–60
   Google Scholar
• Bird A. P. CpG‐rich islands and the function of DNA methylation. Nolure 1986; 321: 209–213
   Google Scholar
• Bishop J. M. The molecular genetics of cancer. Science 1987; 235: 305–311
   PubMed Web of Science ®Google Scholar
• Bond J. V. Bilateral Wilms' tumor; age at diagnosis, associated congenital anomalies and possible pattern of inheritance. Loncer 1975; 2: 482–484
   PubMed Web of Science ®Google Scholar
• Bove K. E., McAdams A. J. The nephroblastomatosis complex and its relationship to Wilms' tumor; a clinicopathologic treatise. Perspect. pedior. Path. 1976; 3: 185–223
   PubMedGoogle Scholar
• Bove K. E., McAdams A. J. Multifocal nephroblastic neoplasia. J. natl. Cancer Inst. 1978; 61: 285–289
   PubMedGoogle Scholar
• Breslow N. E., Beckwith J. B. Epidemiological features of Wilms' tumor; results of the National Wilms' Tumor Study. J. nail. Cancer Inst. 1982; 68: 429–436
   PubMed Web of Science ®Google Scholar
• Brockdorff N., et al. The mapping of a cDNA from the human X‐linked Duchenne muscular dystrophy gene to the mouse X chromosome. Nature 1987; 328: 166–168
   Google Scholar
• Chamberlain J. S., et al. Regional localisation of the murine Duchenne muscular dystrophy gene on the mouse X chromosome. Somatic cell. mol. Genet. 1987; 13: 671–678
   PubMedGoogle Scholar
• Cotlier E., Rose M., Moel S. A. Aniridia, cataracts and Wilms' tumor in monozygous twins. Amer. J. Ophthal. 1978; 86: 129–132
   Google Scholar
• Craver R., Dimmick J., Johnson H., Nigro M. Congenital obstructive uropathy and nodular renal blastema. J. Urol. 1986; 136: 305–307
   PubMed Web of Science ®Google Scholar
• Dao D. D., et al. Genetic mechanisms of tumor‐specific loss of Ilp DNA sequences in Wilms' tumor. Amer. J. hum. Gener. 1987; 41: 202–217
   PubMed Web of Science ®Google Scholar
• Davies K. E., et al. Cloning of a representative genomic library of the human X chromosomes after sorting by flowcytometry. Nature 1981; 293: 374–376
   PubMedGoogle Scholar
• Fearon E. R., Vogelstein B., Feinberg A. P. Somatic deletion and duplication of genes on chromosome 11 in Wilms' turnours. Nature 1984; 309: 176–178
   PubMed Web of Science ®Google Scholar
• Ferrell R. E., et al. Autosomal dominant aniridia; probable linkage to acid phosphatase‐1 locus on chromosome 2. Proc. natl. Acad. Sci. 1980; 77: 1580–1582
   Google Scholar
• Ferrell R. E., Riccardi V. M. Catalase levels in patients with aniridia and/or Wilms' tumor; utility and limitations. Cytogenet. Cell Genet. 1981; 31: 120–123
   Google Scholar
• Flanagan J. C., Digeorge A. M. Sporadic aniridia and Wilms' tumor. Amer. J. Ophthal. 1969; 67: 558–561
   Google Scholar
• Francke U., Holmes L. B., Atkins L., Riccardi V. M. Aniridia‐Wilms' tumor association; evidence for specific deletion of 11p13. Cytogenet. Cell Genet. 1979; 24: 185–192
   PubMedGoogle Scholar
• Fung Y. ‐K.T., et al. Structural evidence for the authenticity of the human retinoblastoma gene. Science 1987; 236: 1657–1661
   PubMed Web of Science ®Google Scholar
• Gateff E. Cancer, genes and development. Adv. Cancer Res. 1982; 37: 33–74
   Google Scholar
• Glaser T., et al. β‐subunit of follicle‐stimulating hormone is deleted in patients with aniridia and Wilms' tumor, allowing a further definition of the WAGR locus. Nature 1987; 321: 882–887
   Google Scholar
• Glaser T. M., et al. Linkage analysis of mouse chromosomes 2, 7 and 19: a comparison with gene order on human chromosomes 11 and 19. Cytogenet. Cell Genet. 1987; 46: 621
   Google Scholar
• Gluecksohn‐Waelsch S., Rota T. R. Development in organ tissue culture of kidney rudiments from mutant mouse embryos. Dev. Biol. 1963; 7: 432–444
   Google Scholar
• Green M. C. Genetic Variants and Strains of the Laboratory Mouse, M. C. Green. Gustav Fischer Verlag. 1981; 217
   Google Scholar
• Gusella J. F., et al. Isolation and characterisation of DNA segments from specific human chromosomes. Proc. natl. Acad. Sci. USA 1980; 77: 2829–2833
   PubMed Web of Science ®Google Scholar
• Haddy T. Nephroblastomatosis: Clinical manifestations and management. Wilms' Tumor: Clinical and Biological Munfyestafions, C. Pochcldy, E. S. Baum. Elsevier. 1984; 111–124
   Google Scholar
• Heideman R. L., McGavran L., Waldstein G. Nephroblastomatosis and deletion of 11p; the potential etiologic relationship to subsequent Wilms' tumor. Amer. J. pediat. Hematol. Oncol. 1986; 8: 231–234
   PubMedGoogle Scholar
• Heilig R., et al. Localisation of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome. Nature 1987; 328: 168–170
   Google Scholar
• Hogan B. L.M., et al. Small eyes (Sey); a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse. J. Embryol. exp. Morph. 1986; 97: 95–110
   PubMedGoogle Scholar
• Hooper M., et al. HPRT deficient (Lesch‐Nyhan) mouse embryos derived from germline colonisation by cultured cells. Nature 1987; 326: 292–294
   PubMed Web of Science ®Google Scholar
• Junien C., et al. Regional assignment of catalase gene to band 11p13; association with aniridia‐Wilms' tumor‐gonadoblastoma complex. Ann. Genet. 1980; 24: 165–168
   Google Scholar
• Klein G. The approaching era of the tumor suppressor genes. Science 1987; 238: 1539–1545
   PubMed Web of Science ®Google Scholar
• Kleinbrecht J. Mouse News Lett. 1974; 51: 19
   Google Scholar
• Knudson A. G., Strong L. C. Mutation and cancer; a model for Wilms' tumor of the kidney. J. Cancer Inst. 1972; 48: 313–324
   PubMed Web of Science ®Google Scholar
• Koenig M., et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organisation of the DMD gene in normal and affected individuals. Cell 1987; 50: 509–517
   PubMed Web of Science ®Google Scholar
• Kolati G. B. Genes and cancer; the story of Wilms' tumor. Science 1980; 207: 970–971
   Google Scholar
• Koufos A., et al. Loss of allelesat loci on human chromosome 11 during genesis of Wilms' tumour. Nature 1984; 309: 170–172
   PubMed Web of Science ®Google Scholar
• Kuehn M. R., Bradley A., Robertson E. J., Evans M. J. A potential animal model for Lesch‐Nyhan syndrome through introduction of HPRT mutations into mice. Nature 1987; 326: 295–298
   PubMed Web of Science ®Google Scholar
• Kulkarni R., et al. Progression of nephroblastomatosis to Wilms' tumor. J. Pediat. 1980; 96: 178
   Google Scholar
• Lee W‐H., Bookstein R., et al. Hunian retinoblastoma susceptibility gene; cloning, identification and sequence. Science 1987a; 235: 1394–1399
   PubMed Web of Science ®Google Scholar
• Lee W‐H., Shew J. ‐H., et al. The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding ability. Nature 1987b; 329: 642–645
   PubMed Web of Science ®Google Scholar
• Martyn L. J., Digeorge A. Selected eye defects of special importance in pediatrics. Pediat. Clins. North Amer. 1987; 34: 1517–1542
   Google Scholar
• Matsunaga E. Genetics of Wilms' tumor. Hum. Genet. 1981; 57: 231–246
   PubMed Web of Science ®Google Scholar
• Meadows A. T., Lichtenfeld J. L., Koop C. E. Wilms' tumor in three children of a woman with congenital hemihypertrophy. Med. Intell. 1974; 291: 23–24
   Google Scholar
• Mechler B. M., McGinnis W., Gehring W. J. Molecular cloning of lethal (2) giant larvae, a recessive oncogene of Drosophila melanogaster. EMBO J. 1985; 4: 1551–1557
   PubMedGoogle Scholar
• Mierau G. W., Beckwith J. B., Weeks D. A. Ultrastructure and histogenesis of the renal tumors of childhood; an overview. Ultrastruct. Path. 1987; 11: 313–333
   PubMed Web of Science ®Google Scholar
• Miller R. W., Fraumeni J. F., Manning M. D. Association of Wilms' tumor with aniridia, hemihypertrophy and other congenital malformations. N. Engl. J. Med. 1964; 270: 922–927
   PubMed Web of Science ®Google Scholar
• Nicholson G. W. Studies on tumour formation. Guy's Hosp. Rep. 1923; 72: 37–64
   Google Scholar
• Orkin S. H., Goldman D. S., Sallan S. E. Development of homozygosity for chromosome 11p markers in Wilms' tumour. Nature 1984; 309: 172–174
   PubMed Web of Science ®Google Scholar
• Porteous D. J. Chromosome mediated gene transfer; a functional assay for complex loci and an aid to human genome mapping. Trends in Genet. 1987; 3: 177–182
   Google Scholar
• Porteous D. J., et al. Hrsal‐selected chromosome transfer generates markers that colocalise aniridia and genitourinary dysplasia‐associated translocation breakpoints and the Wilms' tumor gene within band 11p13. Proc. natl. Acad. Sci. 1987; 84: 5355–5359
   PubMed Web of Science ®Google Scholar
• Potter E. L. Bilateral renal agenesis. J. Pediat. 1946; 29: 68–76
   PubMedGoogle Scholar
• Potter E. L. Normal and Abnormal Development of the Kidney. Year Book, Chicago 1972
   Google Scholar
• Raifer J. Association between Wilms' tumor and gonadal dysgenesis. J. Urol. 1981; 125: 388–390
   Google Scholar
• Raizis A. M. D., Becroft D. M., Shaw R. L., Reeve A. E. A mitotic recombination in Wilms' tumor occurs between the parathyroid hormone locus and 11p13. Hum. Genet. 1985; 7: 344–346
   Google Scholar
• Reeve A. E., et al. Loss of a Harvey ras allele in sporadic Wilms' tumour. Nature 1984; 309: 174–176
   PubMed Web of Science ®Google Scholar
• Riccardi V. M., Sujanski E., Smith A. C., Francke U. Chromosome imbalance in the aniridia‐Wilms' tumor association; 11p interstitial deletion. Pediatrics 1978; 61: 604–610
   PubMed Web of Science ®Google Scholar
• Saxen L. Orgonogenesis of the Kidney. Cambridge University Press. 1987
   Google Scholar
• Schroeder W. T., et al. Nonrandom loss of maternal chromosome 11 alleles in Wilms' tumors. Amer. J. hum. Genet. 1987; 40: 413–420
   PubMed Web of Science ®Google Scholar
• Searle A. G. Mouse Newslett. 1966; 35: 27
   Google Scholar
• Seawright A., et al. Analysis of WACR deletions and related translocations with gene‐specific DNA probes, using FACS‐selected cell hybrids. Somat. cell. mol. Genet. 1988; 14: 21–30
   Google Scholar
• Shaw M. W., Falls H. F., Neel J. V. Congenital aniridia. Amer. J. hum. Genet. 1960; 12: 389–415
   PubMed Web of Science ®Google Scholar
• Simola K. O.J., et al. Familial aniridia and translocation t(4;11)(q22:p13) without Wilms' tumor. Hum. Genet. 1983; 63: 158–161
   Google Scholar
• Southern E. M. Application of DNA analysis to mapping the human genome. Cytogener. cell. Genet. 1982; 32: 52–57
   PubMedGoogle Scholar
• Stern R. J., Hunter W. S., Moross T., Gardner H. A. Prenatal diagnosis of del(11)(p13p15). Prenatal Diagn. 1988; 8: 1–6
   Google Scholar
• Surani M. A. H. Experimental Approaches to Mammalian Embryonic Development, J. Rossant, R. A. Pedersen. Cambridge University Press. 1981; 401–436
   Google Scholar
• Theiler K., Vaknum D. S., Stevens L. C. Development of Dickies small eye, a mutation in the house mouse. Anat. Embryol. 1978; 155: 81–86
   Google Scholar
• Turleau C., et al. Del11p13/nephroblastoma without aniridia. Hum. Genet. 1984; 67: 455–456
   Google Scholar
• van Heyningen V., et al. Molecular analysis of chromosome 11 deletions in aniridia‐Wilms' tumor syndrome. Proc. natl. Acad. Sci. 1985; 82: 8592–8596
   PubMed Web of Science ®Google Scholar
• Weissman B. E., et al. Introduction of a normal human chromosome 11 into a Wilms' tumor cell line controls its tumorigenic expression. Science 1987; 236: 175–180
   PubMed Web of Science ®Google Scholar
• Wilkins R. J. Genornic imprinting and carcinogenesis. Lancet 1988; 1: 329–331
   PubMed Web of Science ®Google Scholar