The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21
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Citations
Cites
Cox, D. R., Burmeister, M., Price, E. R., Kim, S., & Myers, R. M. (1990) · Science · doi:10.1126/science.2218528 · Cited by 621
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
Rahmani, Z., Blouin, J. L., Creau-Goldberg, N., Watkins, P. C., Mattei, J. F., Poissonnier, M., Prieur, M., Chettouh, Z., Nicole, A., & Aurias, A. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.15.5958 · Cited by 258
Self-citationKorenberg, J. R., Kawashima, H., Pulst, S. M., Ikeuchi, T., Ogasawara, N., Yamamoto, K., Schonberg, S. A., West, R. J., Allen, L., & Magenis, E. (1990) · PubMed · Cited by 242
Molecular genetic approach to the characterization of the “Down syndrome region” of chromosome 21
McCormick, M. K., Schinzel, A., Petersen, M. B., Stetten, G., Driscoll, D. J., Cantu, E. S., Tranebjaerg, L., Mikkelsen, M., Watkins, P. C., & Antonarakis, S. E. (1989) · Genomics · doi:10.1016/0888-7543(89)90065-7 · Cited by 195
Rao, V. N., Papas, T. S., & Reddy, E. S. P. (1987) · Science · doi:10.1126/science.3299708 · Cited by 176
Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.
Korenberg, J. R., Bradley, C. M., & Distèche, C. M. (1992) · Europe PMC (PubMed Central) · Cited by 175
Trisomie 21 et superoxyde dismutase-1 (IPO-A)
Sinet, P.-M., Couturier, J., Dutrillaux, B., Poissonnier, M., Raoul, O., Rethoré, M.-O., Allard, D., Lejeune, J., & Jerome, H. (1976) · Experimental Cell Research · doi:10.1016/0014-4827(76)90653-4 · Cited by 175
Self-citationProtocols to establish genotype-phenotype correlations in Down syndrome.
Epstein, C. J., Korenberg, J. R., Annerén, G., Antonarakis, S. E., Aymé, S., Courchesne, E., Epstein, L. B., Fowler, A. E., Groner, Y., & Huret, J. L. (1991) · PubMed · Cited by 145
Burmeister, M., Kim, S., Price, E. R., de Lange, T., Tantravahi, U., Myers, R., & Cox, D. (1991) · Genomics · doi:10.1016/0888-7543(91)90216-2 · Cited by 123
Report of the Second International Workshop on Human Chromosome 6
Volz, A., Boyle, J. M., Cann, H. M., Cottingham, R. W., Orr, H. T., & Ziegler, A. (1994) · Genomics · doi:10.1006/geno.1994.1302 · Cited by 109
Cited by
Down syndrome phenotypes: the consequences of chromosomal imbalance.
Korenberg, J. R., Chen, X. N., Schipper, R., Sun, Z., Gonsky, R., Gerwehr, S., Carpenter, N., Daumer, C., Dignan, P., & Disteche, C. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.4997 · Cited by 784
Chromosome 21 and Down syndrome: from genomics to pathophysiology
Antonarakis, S. E., Lyle, R., Dermitzakis, E. T., Reymond, A., & Deutsch, S. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1448 · Cited by 703
An Aneuploid Mouse Strain Carrying Human Chromosome 21 with down Syndrome Phenotypes.
O'Doherty, A., Ruf, S., Mulligan, C., Hildreth, V., Errington, M. L., Cooke, S., Sesay, A., Modino, S., Vanes, L., Hernandez, D., et al. (2005) · Science · doi:10.1126/science.1114535 · Cited by 434
Korbel, J. O., Tirosh-Wagner, T., Urban, A. E., Chen, X.-N., Kasowski, M., Dai, L., Grubert, F., Erdman, C., Gao, M. C., Lange, K., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813248106 · Cited by 399
Altafaj, X. (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.18.1915 · Cited by 396
Metadata
- Authors
- Delabar, J.-M., Theophile, D., Rahmani, Z., Chettouh, Z., Blouin, J.-L., Prieur, M., Noel, B., & Sinet, P.-M.
- Venue
- European Journal of Human Genetics
- Published
- 1993
- Volume
- 1
- Issue
- 2
- Pages
- 114-124
- ISSN
- 1018-4813 (ISSN-L)
- 1476-5438
- OpenAlex
- W1860217789
- Cited by
- 451
- References
- 26
- FWCI
- 17.15
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21. https://app.cochat.ai/papers/10.1159/000472398
- The paper
- Delabar, J.-M., Theophile, D., Rahmani, Z., Chettouh, Z., Blouin, J.-L., Prieur, M., Noel, B., & Sinet, P.-M. (1993). Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21. European Journal of Human Genetics. https://doi.org/10.1159/000472398
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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.
