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Canning, S., Dryja, T. P. (1989) Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene. Proceedings of the National Academy of Sciences, 86 (13) 5044-5048 doi:10.1073/pnas.86.13.5044

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Reference TypeJournal (article/letter/editorial)
TitleShort, direct repeats at the breakpoints of deletions of the retinoblastoma gene.
JournalProceedings of the National Academy of Sciences
AuthorsCanning, S.Author
Dryja, T. P.Author
Year1989 (July 1)Volume86
Issue13
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.86.13.5044Search in ResearchGate
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Mindat Ref. ID1475395Long-form Identifiermindat:1:5:1475395:4
GUID0
Full ReferenceCanning, S., Dryja, T. P. (1989) Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene. Proceedings of the National Academy of Sciences, 86 (13) 5044-5048 doi:10.1073/pnas.86.13.5044
Plain TextCanning, S., Dryja, T. P. (1989) Short, direct repeats at the breakpoints of deletions of the retinoblastoma gene. Proceedings of the National Academy of Sciences, 86 (13) 5044-5048 doi:10.1073/pnas.86.13.5044
In(1989, July) Proceedings of the National Academy of Sciences Vol. 86 (13) Proceedings of the National Academy of Sciences

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Bernards, R, Schackleford, G M, Gerber, M R, Horowitz, J M, Friend, S H, Schartl, M, Bogenmann, E, Rapaport, J M, McGee, T, Dryja, T P (1989) Structure and expression of the murine retinoblastoma gene and characterization of its encoded protein. Proceedings of the National Academy of Sciences, 86 (17) 6474-6478 doi:10.1073/pnas.86.17.6474
Dryja, T. P. (1997) Gene-based approach to human gene-phenotype correlations. Proceedings of the National Academy of Sciences, 94 (22) 12117-12121 doi:10.1073/pnas.94.22.12117
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
Bernards, R., Shackleford, G. M., Gerber, M. R., Horowitz, J. M., Friend, S. H., Schartl, M., Bogenmann, E., Rapaport, J. M., McGee, T., Dryja, T. P., Weinberg, R. A. (2006) Correction for Bernards et al., Structure and Expression of the Murine Retinoblastoma Gene and Characterization of its Encoded Protein, PNAS 1989 86:6474-6478. Proceedings of the National Academy of Sciences, 103 (5) 1656 doi:10.1073/pnas.0510340102
Larsen, N. (1992) Higher order interactions in 23s rRNA. Proceedings of the National Academy of Sciences, 89 (11) 5044-5048 doi:10.1073/pnas.89.11.5044
Squire, J., Dryja, T. P., Dunn, J., Goddard, A., Hofmann, T., Musarella, M., Willard, H. F., Becker, A. J., Gallie, B. L., Phillips, R. A. (1986) Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. Proceedings of the National Academy of Sciences, 83 (17) 6573-6577 doi:10.1073/pnas.83.17.6573
Shapiro, L. J., Yen, P., Pomerantz, D., Martin, E., Rolewic, L., Mohandas, T. (1989) Molecular studies of deletions at the human steroid sulfatase locus. Proceedings of the National Academy of Sciences, 86 (21) 8477-8481 doi:10.1073/pnas.86.21.8477
Ryan, S. C., Dugaiczyk, A. (1989) Newly arisen DNA repeats in primate phylogeny. Proceedings of the National Academy of Sciences, 86 (23) 9360-9364 doi:10.1073/pnas.86.23.9360
(1989) Correction: Mutator Phenotype of Werner Syndrome is Characterized by Extensive Deletions. Proceedings of the National Academy of Sciences, 86 (20) 7994 doi:10.1073/pnas.86.20.7994
Ballinger, D. G., Benzer, S. (1989) Targeted gene mutations in Drosophila. Proceedings of the National Academy of Sciences, 86 (23) 9402-9406 doi:10.1073/pnas.86.23.9402
Dryja, T. P., Hahn, L. B., Cowley, G. S., McGee, T. L., Berson, E. L. (1991) Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa. Proceedings of the National Academy of Sciences, 88 (20) 9370-9374 doi:10.1073/pnas.88.20.9370
 
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