This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study
Molecular Autism Open Access 23 June 2020
-
Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
Molecular Cytogenetics Open Access 12 August 2016
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Greenberg, F. Am. J. Med. Genet. (suppl.), 6, 85–88 (1993).
Ewart, A.K. et al. Nature Genet. 5, 11–16 (1993).
Morris, C.A., Thomas, I.T. & Greenberg, F. Am. J. Med. Genet. 47, 478–481 (1993).
Nickerson, E., Greenberg, F., Keating, M., McCaskill, C. & Shaffer, L.G. Am. J. Hum. Genet. 56, 1156–1161 (1995).
Lowery, M.C. et al. Am. J. Hum. Genet. 57, 49–53 (1995).
Morris, C.A., Demsey, S.A., Leonard, C.O., Dilts, C. & Blackburn, B.L. J. Pediatr. 113, 318–326 (1988).
Morris, C.A., Loker, J., Ensing, G. & Stock, A.D. Am. J. Med. Genet. 46, 737–744 (1993).
Curran, M.E. et al. Cell 73, 159–168 (1993).
Mizuno, K. et al. Oncogene 9, 1605–1612 (1994).
Pröschel, C., Blouin, M.-J., Gutowski, N.J., Ludwig, R. & Noble, M. Oncogene 11, 1271–1281 (1995).
Taira, M., Evrard, J.-L., Steinmetz, A. & Dawid, I.B. Trends Genet. 11, 431–432 (1995).
Nunoue, K., Ohashi, K., Okano, I. & Mizuno, K. Oncogene 11, 701–710 (1995).
Pinkel, D. et al. Proc. Natl. Acad. Sci. USA 85, 9138–9142 (1988).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Tassabehji, M., Metcalfe, K., Fergusson, W. et al. LIM–kinase deleted in Williams syndrome. Nat Genet 13, 272–273 (1996). https://doi.org/10.1038/ng0796-272
Issue Date:
DOI: https://doi.org/10.1038/ng0796-272
This article is cited by
-
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study
Molecular Autism (2020)
-
Aberrant expression of LIMK1 impairs neuronal migration during neocortex development
Histochemistry and Cell Biology (2017)
-
Genome wide array-CGH and qPCR analysis for the identification of genome defects in Williams’ syndrome patients in Saudi Arabia
Molecular Cytogenetics (2016)
-
Dendritic spine abnormalities in mental retardation
Cell and Tissue Research (2010)
-
Rho-linked genes and neurological disorders
Pflügers Archiv - European Journal of Physiology (2008)