Abstract
The family of four fibroblast growth factor receptors is stimulating attention with the discovery of genetic defects tying three members to a variety of congenital bone malformations.
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References
Shiang, R. et al. Cell 78, 335–342 (1994).
Rousseau, F. et al. Nature 371, 252–254 (1994).
Reardon, W. et al. Nature Genet. 8, 98–103 (1994).
Muenke, M. et al. Nature Genet. 8, 269–274 (1994).
Jabs, E. W. et al. Nature Genet. 8, 275–279 (1994).
Mason, I. J. Cell 78, 547–552 (1994).
Ichinose, H. et al. Nature Genet 8, 236–242 (1994).
Kawaguchi, Y. et al. Nature Genet. 8, 221–228 (1994).
Ranum, L. P. W., Schut, L. J., Lundgren, J. K., Orr, H. T. & Livingston, D. M. Nature Genet. 8, 280–284 (1994).
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Davies, K. Receptor malfunction. Nature 372, 202 (1994). https://doi.org/10.1038/372202a0
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DOI: https://doi.org/10.1038/372202a0