This is a preview of subscription content, log in via an institution to check access.
References
Balling, R., Mutter, G., Gruss, P., Kessel, M. (1989). Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice. Cell 58, 337–347.
Bastian, H., Gruss, P., Duboule, D., Izpisua-Belmonte, J.-C. (1992). The murine even-skipped-like gene Evx-2 is closely linked to the Hox-4 complex, but is transcribed in the opposite direction. Mamm. Genome 3, 241–243.
Dietrich, W., Katz, H., Lincoln, S.E., Shin, H.-S., Friedman, J., Dracopoli, N.C., Lander, E.S. (1992). A genetic map of the mouse suitable for typing intraspecific crosses. Genetics 131, 423–447.
Dixon, M.J., Read, A.P., Donnai, D., Colley, A., Dixon, J., Williamson, R. (1991). The gene for Treacher Collins syndrome maps to the long arm of chromosome 5. Am. J. Hum. Genet. 49, 17–22.
Dolle, P., Price, M., Duboule, D. (1992) Expression of the murine D/x-1 homeobox gene during facial, ocular and limb development. Differentiation 49, 93–99.
Flaherty, L. (1981). Congenic strains. In The Mouse in Biomedical Research, Vol. 1, H.L. Foster, J.D. Small, J.G. Fox, eds. (New York, N.Y.: Academic Press), pp. 215–222.
Harris, M.J., Juriloff, D.M. (1989). Test of the isoallele hypothesis at the mouse First arch (far) locus. J. Hered. 80, 127–131.
Harris, M.J., Juriloff, D.M., Peters, C.E. (1990). Disruption of pattern formation in palatal rugae in fetal mice heterozygous for First arch (Far). J. Craniofac. Genet. Dev. Biol. 10, 363–371.
Jones, K.L. (1988). Smith's Recognizable Patterns of Human Malformation, 4th ed. (Philadelphia: W.B. Saunders Co.).
Juriloff, D.M., Harris, M.J. (1983). Abnormal facial development in the mouse mutant first arch. J. Craniofac. Genet. Dev. Biol. 3, 317–337.
Juriloff, D.M., Harris, M.J. (1991). Mapping the mouse craniofacial mutation First arch (Far) to chromosome 2. J. Hered. 82, 402–405.
Juriloff, D.M., Harris, M.J., Froster-Iskenius, U. (1987). Hemifacial deficiency induced by a shift in dominance of the mouse mutation far: a possible genetic model for hemifacial microsomia. J. Craniofac. Genet. Dev. Biol. 7, 27–44.
Juriloff, D.M., Harris, M.J., Miller, J.E., Jacobson, D., Martin, P. (1992). Is Far a Hox mutation? J. Craniofac. Genet. Dev. Biol. 12, 119–129.
Kaur, S., Singh, G., Stock, J.L., Schreiner, C.M., Kier, A.B., Yager, K.L., Mucenski, M.L., Scott, W.J., Potter, S.S. (1992). Dominant mutation of the murine Hox-2.2 gene results in developmental abnormalities. J. Exp. Zool. 264, 323–336.
Kessel, M., Balling, R., Gruss, P. (1990). Variations of cervical vertebrae after expression of a Hox-1.1 transgene in mice. Cell 61, 301–308.
Krumlauf, R. (1993). Hox genes and pattern formation in the branchial region of the vertebrate head. Trends Genet. 9, 106–112.
Lufkin, T., Mark, M., Hart, C.P., Dolle, P., LeMeur, M., Chambon, P. (1992). Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene. Nature 359, 835–841.
McLeod, M.J., Harris, M.J., Chernoff, G.F., Miller, J.R. (1980). First arch malformation: a new craniofacial mutant in the mouse. J. Hered. 71, 331–335.
Morgan, B.A., Izpisua-Belmonte, J.-C., Duboule, D., Tabin, C.J. (1992). Targeted misexpression of Hox-4.6 in the avian limb bud causes apparent homeotic transformations. Nature 358, 236–239.
Peichel, C.L., Scherer, S.W., Tsui, L.-C., Beier, D.R., Vogt, T.F. (1993). Mapping the midkine family of developmentally regulated signaling molecules. Mamm. Genome 4, 632–638.
Porteus, M.H., Bulfone, A., Ciaranello, R.D., Rubenstein, J.L.R. (1991). Isolation and characterization of a novel cDNA clone encoding a homeodomain that is developmentally regulated in the ventral forebrain. Neuron 7, 221–229.
Sambrook, J., Fritsch, E.F., Maniatis, T.M. (1989). Molecular Cloning: A Laboratory Manual, 2nd ed. (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press).
Siracusa, L.D., Abbott, C.M. (1993). Mouse Chromosome 2. Mamm. Genome 4(Suppl.), S31-S46.
Spurr, N.K., Cox, S., Naylor, S. (1993). Report of the second international workshop on human chromosome 2 mapping. Cytogenet. Cell Genet. 64, 70–85.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Juriloff, D.M., Harris, M.J. & Mah, D.G. Mapping Far (First arch) in relation to molecular markers on mouse Chromosome 2. Mammalian Genome 5, 450–452 (1994). https://doi.org/10.1007/BF00357007
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00357007