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van Heyningen, V., Boyd, P. A., Seawright, A., Fletcher, J. M., Fantes, J. A., Buckton, K. E., Spowart, G., Porteous, D. J., Hill, R. E., Newton, M. S. (1985) Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. Proceedings of the National Academy of Sciences, 82 (24) 8592-8596 doi:10.1073/pnas.82.24.8592

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Reference TypeJournal (article/letter/editorial)
TitleMolecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
JournalProceedings of the National Academy of Sciences
Authorsvan Heyningen, V.Author
Boyd, P. A.Author
Seawright, A.Author
Fletcher, J. M.Author
Fantes, J. A.Author
Buckton, K. E.Author
Spowart, G.Author
Porteous, D. J.Author
Hill, R. E.Author
Newton, M. S.Author
Year1985 (December 1)Volume82
Issue24
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.82.24.8592Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1446454Long-form Identifiermindat:1:5:1446454:6
GUID0
Full Referencevan Heyningen, V., Boyd, P. A., Seawright, A., Fletcher, J. M., Fantes, J. A., Buckton, K. E., Spowart, G., Porteous, D. J., Hill, R. E., Newton, M. S. (1985) Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. Proceedings of the National Academy of Sciences, 82 (24) 8592-8596 doi:10.1073/pnas.82.24.8592
Plain Textvan Heyningen, V., Boyd, P. A., Seawright, A., Fletcher, J. M., Fantes, J. A., Buckton, K. E., Spowart, G., Porteous, D. J., Hill, R. E., Newton, M. S. (1985) Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. Proceedings of the National Academy of Sciences, 82 (24) 8592-8596 doi:10.1073/pnas.82.24.8592
In(1985, December) Proceedings of the National Academy of Sciences Vol. 82 (24) Proceedings of the National Academy of Sciences

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Porteous, D. J., Bickmore, W., Christie, S., Boyd, P. A., Cranston, G., Fletcher, J. M., Gosden, J. R., Rout, D., Seawright, A., Simola, K. O. (1987) HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13. Proceedings of the National Academy of Sciences, 84 (15) 5355-5359 doi:10.1073/pnas.84.15.5355
van Heyningen, V., Bickmore, W. A., Seawright, A., Fletcher, J. M., Maule, J., Fekete, G., Gessler, M., Bruns, G. A., Huerre-Jeanpierre, C., Junien, C. (1990) Role for the Wilms tumor gene in genital development?. Proceedings of the National Academy of Sciences, 87 (14) 5383-5386 doi:10.1073/pnas.87.14.5383
Little, M. H., Prosser, J., Condie, A., Smith, P. J., Van Heyningen, V., Hastie, N. D. (1992) Zinc finger point mutations within the WT1 gene in Wilms tumor patients. Proceedings of the National Academy of Sciences, 89 (11) 4791-4795 doi:10.1073/pnas.89.11.4791
Prawitt, D., Enklaar, T., Gartner-Rupprecht, B., Spangenberg, C., Oswald, M., Lausch, E., Schmidtke, P., Reutzel, D., Fees, S., Lucito, R., Korzon, M., Brozek, I., Limon, J., Housman, D. E., Pelletier, J., Zabel, B. (2005) Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor. Proceedings of the National Academy of Sciences, 102 (11) 4085-4090 doi:10.1073/pnas.0500037102
Paige, A. J. W., Taylor, K. J., Taylor, C., Hillier, S. G., Farrington, S., Scott, D., Porteous, D. J., Smyth, J. F., Gabra, H., Watson, J. E. V. (2001) WWOX: A candidate tumor suppressor gene involved in multiple tumor types. Proceedings of the National Academy of Sciences, 98 (20) 11417-11422 doi:10.1073/pnas.191175898
Karayiorgou, M., Morris, M. A., Morrow, B., Shprintzen, R. J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P. S., Lasseter, V. K. (1995) Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proceedings of the National Academy of Sciences, 92 (17) 7612-7616 doi:10.1073/pnas.92.17.7612
Lauderdale, J. D., Wilensky, J. S., Oliver, E. R., Walton, D. S., Glaser, T. (2000) 3' deletions cause aniridia by preventing PAX6 gene expression. Proceedings of the National Academy of Sciences, 97 (25) 13755-13759 doi:10.1073/pnas.240398797
Little, J. W., Hill, S. A. (1985) Deletions within a hinge region of a specific DNA-binding protein. Proceedings of the National Academy of Sciences, 82 (8) 2301-2305 doi:10.1073/pnas.82.8.2301
Dryja, T. P., Rapaport, J. M., Joyce, J. M., Petersen, R. A. (1986) Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas. Proceedings of the National Academy of Sciences, 83 (19) 7391-7394 doi:10.1073/pnas.83.19.7391
Haber, D. A., Sohn, R. L., Buckler, A. J., Pelletier, J., Call, K. M., Housman, D. E. (1991) Alternative splicing and genomic structure of the Wilms tumor gene WT1. Proceedings of the National Academy of Sciences, 88 (21) 9618-9622 doi:10.1073/pnas.88.21.9618
Ledbetter, D. H., Ledbetter, S. A., vanTuinen, P., Summers, K. M., Robinson, T. J., Nakamura, Y., Wolff, R., White, R., Barker, D. F., Wallace, M. R. (1989) Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region. Proceedings of the National Academy of Sciences, 86 (13) 5136-5140 doi:10.1073/pnas.86.13.5136
 
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