The DOI matches its Crossref record.
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
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Citations
Cited by
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
Satokata, I., Ma, L., Ohshima, H., Bei, M., Woo, I., Nishizawa, K., Maeda, T., Takano, Y., Uchiyama, M., Heaney, S., et al. (2000) · Nature Genetics · doi:10.1038/74231 · Cited by 737
Self-citationMorriss‐Kay, G. M., & Wilkie, A. O. M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00475.x · Cited by 483
Johnson, D., & Wilkie, A. O. M. (2011) · European Journal of Human Genetics · doi:10.1038/ejhg.2010.235 · Cited by 499
Lecanda, F., Warlow, P. M., Sheikh, S., Furlan, F., Steinberg, T. H., & Civitelli, R. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.151.4.931 · Cited by 395
Genetic study of nonsyndromic coronal craniosynostosis
Lajeunie, E., Merrer, M. L., Bonaïti‐Pellie, C., Marchac, D., & Renier, D. (1995) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320550422 · Cited by 374
Metadata
- Authors
- Jabs, E. W., Müller, U., Li, X., Ma, L., Luo, W., Haworth, I. S., Klisak, I., Sparkes, R., Warman, M. L., Mulliken, J. B., Snead, M. L., & Maxson, R.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1993-11
- Volume
- 75
- Issue
- 3
- Pages
- 443-450
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2170516128
- Cited by
- 677
- References
- 0
- FWCI
- 19.01
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
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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How to cite
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- This page
- CoChat. (2026). Citation check: A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. https://app.cochat.ai/papers/10.1016/0092-8674(93)90379-5
- The paper
- Jabs, E. W., Müller, U., Li, X., Ma, L., Luo, W., Haworth, I. S., Klisak, I., Sparkes, R., Warman, M. L., Mulliken, J. B., Snead, M. L., & Maxson, R. (1993). A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell. https://doi.org/10.1016/0092-8674(93)90379-5
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.
