The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
High resolution visual mapping of stretched DNA by fluorescent hybridization
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Citations
Cites
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.
Pinkel, D., Straume, T., & Gray, J. W. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.9.2934 · Cited by 3,219
High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones
Lichter, P., Tang, C.-J. C., Call, K., Hermanson, G., Evans, G. A., Housman, D., & Ward, D. C. (1990) · Science · doi:10.1126/science.2294592 · Cited by 1,331
Cox, D. R., Burmeister, M., Price, E. R., Kim, S., & Myers, R. M. (1990) · Science · doi:10.1126/science.2218528 · Cited by 621
High-resolution mapping of mammalian genes by in situ hybridization to free chromatin.
Heng, H. H., Squire, J., & Tsui, L. C. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.20.9509 · Cited by 516
Interphase and Metaphase Resolution of Different Distances Within the Human Dystrophin Gene
Lawrence, J. B., Singer, R. H., & McNeil, J. A. (1990) · Science · doi:10.1126/science.2203143 · Cited by 257
Windle, B., Draper, B. W., Yin, Y. X., O'Gorman, S., & Wahl, G. M. (1991) · Genes & Development · doi:10.1101/gad.5.2.160 · Cited by 242
Self-citationEstimating Genomic Distance from DNA Sequence Location in Cell Nuclei by a Random Walk Model
van den Engh, G., Sachs, R., & Trask, B. J. (1992) · Science · doi:10.1126/science.1388286 · Cited by 240
Green, E. D., & Olson, M. V. (1990) · Science · doi:10.1126/science.2218515 · Cited by 236
Trask, B., Pinkel, D., & van den Engh, G. (1989) · Genomics · doi:10.1016/0888-7543(89)90112-2 · Cited by 224
Effect of gamma rays at the dihydrofolate reductase locus: Deletions and inversions
Urlaub, G., Mitchell, P. J., Kas, E., Chasin, L. A., Funanage, V. L., Myoda, T. T., & Hamlin, J. (1986) · Somatic Cell and Molecular Genetics · doi:10.1007/bf01671941 · Cited by 222
Cited by
Smith, S. B., Cui, Y., & Bustamante, C. (1996) · Science · doi:10.1126/science.271.5250.795 · Cited by 2,770
Structural variation in the human genome
Feuk, L., Carson, A. R., & Scherer, S. W. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1767 · Cited by 2,034
Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
Petrif, F., Giles, R. H., Dauwerse, H. G., Saris, J. J., Hennekam, R. C. M., Masuno, M., Tommerup, N., van Ommen, G.-J. B., Goodman, R. H., Peters, D. J. M., et al. (1995) · Nature · doi:10.1038/376348a0 · Cited by 1,217
The new cytogenetics: blurring the boundaries with molecular biology
Speicher, M. R., & Carter, N. P. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1692 · Cited by 458
Structural Variation of the Human Genome
Sharp, A. J., Cheng, Z., & Eichler, E. E. (2006) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.7.080505.115618 · Cited by 293
Metadata
- Authors
- Parra, I., & Windle, B.
- Venue
- Nature Genetics
- Published
- 1993-09
- Volume
- 5
- Issue
- 1
- Pages
- 17-21
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1991713583
- Cited by
- 290
- References
- 15
- FWCI
- 10.11
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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- CoChat. (2026). Citation check: High resolution visual mapping of stretched DNA by fluorescent hybridization. https://app.cochat.ai/papers/10.1038/ng0993-17
- The paper
- Parra, I., & Windle, B. (1993). High resolution visual mapping of stretched DNA by fluorescent hybridization. Nature Genetics. https://doi.org/10.1038/ng0993-17
Data sources
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.