The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.
Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction
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Citations
Cites
PCR protocols — A guide to methods and applications
(1990) · Trends in Genetics · doi:10.1016/0168-9525(90)90186-a · Cited by 11,781
Koenig, M., Hoffman, E. P., Bertelson, C. J., Monaco, A. P., Feener, C., & Kunkel, L. M. (1987) · Cell · doi:10.1016/0092-8674(87)90504-6 · Cited by 2,411
Self-citationThe complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
Koenig, M., Monaco, A. P., & Kunkel, L. M. (1988) · Cell · doi:10.1016/0092-8674(88)90383-2 · Cited by 1,538
Self-citationAnalysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
Kunkel, L. M., Smith, K. D., Boyer, S. H., Borgaonkar, D. S., Wachtel, S. S., Miller, O. J., Breg, W. R., Jones, H. W., & Rary, J. M. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.3.1245 · Cited by 1,334
Self-citationDeletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
Chamberlain, J. S., Gibbs, R. A., Rainer, J. E., Nguyen, P. N., & Thomas, C. (1988) · Nucleic Acids Research · doi:10.1093/nar/16.23.11141 · Cited by 1,262
Monaco, A. P., Bertelson, C. J., Liechti-Gallati, S., Moser, H., & Kunkel, L. M. (1988) · Genomics · doi:10.1016/0888-7543(88)90113-9 · Cited by 1,210
Self-citationKoenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kääriäinen, H. A., et al. (1989) · Europe PMC (PubMed Central) · Cited by 961
Self-citationHoffman, E. P., Fischbeck, K. H., Brown, R. H., Johnson, M., Medori, R., Loire, J. D., Harris, J. B., Waterston, R., Brooke, M., Specht, L., et al. (1988) · New England Journal of Medicine · doi:10.1056/nejm198805263182104 · Cited by 927
Self-citationSAMPLE PREPARATION FROM BLOOD, CELLS, AND OTHER FLUIDS
Kawasaki, E. S. (1990) · PCR Protocols · doi:10.1016/b978-0-12-372180-8.50022-6 · Cited by 421
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
Hoffman, E. P., & Kunkel, L. M. (1989) · Neuron · doi:10.1016/0896-6273(89)90226-2 · Cited by 331
Self-citationImproved diagnosis of Becker muscular dystrophy by dystrophin testing
Hoffman, E. P., Kunkel, L. M., Angelini, C., Clarke, A., Johnson, M., & Harris, J. B. (1989) · Neurology · doi:10.1212/wnl.39.8.1011 · Cited by 291
Self-citationFrame-Shift Deletions in Patients with Duchenne and Becker Muscular Dystrophy
Malhotra, S. B., Hart, K. A., Klamut, H. J., Thomas, N. S. T., Bodrug, S. E., Burghes, A. H. M., Bobrow, M., Harper, P. S., Thompson, M. W., Ray, P. N., et al. (1988) · Science · doi:10.1126/science.3055295 · Cited by 284
MULTIPLEX PCR FOR THE DIAGNOSIS OF DUCHENNE MUSCULAR DYSTROPHY
Chamberlain, J. S., Gibbs, R. A., Ranier, J. E., & Caskey, C. T. (1990) · PCR Protocols · doi:10.1016/b978-0-12-372180-8.50037-8 · Cited by 225
Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies
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Gillard, E. F., Chamberlain, J. S., Murphy, E. G., Duff, C. L., Smith, B. A., Burghes, A. H. M., Thompson, M. W., Sutherland, J. S., Oss, I., & Bodrug, S. (1989) · Europe PMC (PubMed Central) · Cited by 184
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
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Improved diagnosis of Duchenne/Becker muscular dystrophy.
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Self-citationRapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy
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Cited by
Disease-Specific Induced Pluripotent Stem Cells.
Park, I.-H., Arora, N., Huo, H., Maherali, N., Ahfeldt, T., Shimamura, A., Lensch, M. W., Cowan, C., Hochedlinger, K., & Daley, G. Q. (2008) · Cell · doi:10.1016/j.cell.2008.07.041 · Cited by 2,196
“Multiplex PCR analysis with primer sets amplifying several (but not all) intragenic intervals of the dystrophin gene (Beggs et al., 1990; Chamberlain et al., 1988) revealed the deletion of exons 45–52 in the iPS cells derived from a patient with Duchenne muscular dystrophy (DMD; Figure 1C).”
Zhu, H., Zhang, H., Xu, Y., Laššáková, S., Korabečná, M., & Neužil, P. (2020) · BioTechniques · doi:10.2144/btn-2020-0057 · Cited by 380
The importance of genetic diagnosis for Duchenne muscular dystrophy
Aartsma-Rus, A., Ginjaar, I. B., & Bushby, K. (2016) · Journal of Medical Genetics · doi:10.1136/jmedgenet-2015-103387 · Cited by 369
Metadata
- Authors
- Beggs, A., Koenig, M., Boyce, F., & Kunkel, L.
- Venue
- Human Genetics
- Published
- 1990-11
- Volume
- 86
- Issue
- 1
- Pages
- 45-8
- ISSN
- 0018-7348 (ISSN-L)
- 0340-6717
- 1432-1203
- OpenAlex
- W1997140189
- Cited by
- 688
- References
- 18
- FWCI
- 13.24
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.