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-citation
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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- CoChat. (2026). Citation check: Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. https://app.cochat.ai/papers/10.1007/bf00205170
- The paper
- Beggs, A., Koenig, M., Boyce, F., & Kunkel, L. (1990). Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction. Human Genetics. https://doi.org/10.1007/bf00205170
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
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.
