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Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene

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References

  • Angel, T.A., Faust, C.J., Gonzales, J.C., Kenwrick, S., Lewis, R.A., Herman, G.E. (1993). Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28. Mamm. Genome 4, 171–176.

    Google Scholar 

  • Bawle, E., Tyrkus, M., Lipman, S., Bozimowski, D. (1984). Aarskog syndrome: full male and female expression associated with an X-autosome translocation. Am. J. Med. Genet. 17, 595–602.

    Google Scholar 

  • Blair, H.J., Reed, V., Lavak, S.H., Boyd, Y. (1994). New insights into the man-mouse comparative map of the X chromosome. Genomics 19, 215–220.

    Google Scholar 

  • Boguski, M.S., McCormick, F. (1993). Proteins regulating Ras and its relatives. Nature 366, 643–653.

    Google Scholar 

  • Chapman, V.M., Keitz, B.T., Bishop, D.F. (1994). Genetic linkage of the erythroid-specific delta-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X chromosome. Mamm. Genome 5, 714.

    Google Scholar 

  • Devereux, J., Haeberli, P., Smithies, O. (1984). A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 12, 387–395.

    Google Scholar 

  • Glover, T.W., Verga, V., Rafael, J., Gorski, J.L., Bawle, E., Higgins, J.V. (1993). Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Hum. Mol. Genet. 10, 1717–1718.

    Google Scholar 

  • Gorlin, R.J., Cohen, M.M., Levin, L.S. (1990). Syndromes of the Head and Neck, 3rd ed. (New York, N.Y. Oxford University Press), pp. 295–297.

    Google Scholar 

  • Gorski, J.L., Boehnke, M., Reyner, E.L., Burright, E.N. (1992). A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti (IP1) translocation breakpoints. Genomics 14, 657–665.

    Google Scholar 

  • Herman, G.E., Walton, S.J. (1990). Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics 7, 307–312.

    Google Scholar 

  • Herman, G.E., Boyd, Y., Chapman, V., Chatterjee, A., Brown, S.D.M. (1994). Mouse X chromosome. Mamm. Genome 5 (suppl.), S276-S288.

    Google Scholar 

  • Lyon, M.F., Searle, A.G. (1989). Genetic Variants and Strains of the Laboratory Mouse, 2nd ed. (New York, N.Y.: Oxford University Press).

    Google Scholar 

  • Pasteris, N.G., Cadle A., Logie L.J., Porteous M.E.M., Schwartz, C.E., Stevenson R.E., Glover, T.W., Wilroy, R., Gorski, J.L. (1994). Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor. Cell 79, 669–678.

    Google Scholar 

  • Porteous, M.E.M., Goudie, D.R. (1991). Aarskog syndrome. J. Med. Genet. 28, 44–47.

    Google Scholar 

  • Porteous, M.E.M., Curtis, A., Lindsay, S., Williams, O., Goudie, D., Kamakari, S., Bhattacharya, S.S. (1992). The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13). Genomics 14, 298–301.

    Google Scholar 

  • Stevenson, R.E., May, M., Arena, J.F., Millar, E.A., Scott, Jr. C.I. (1994). Aarskog-Scott syndrome: confirmation of linkage to the pericentric region of the X chromosome. Am. J. Med. Genet. 52, 339–345.

    Google Scholar 

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Pasteris, N.G., de Gouyon, B., Cadle, A.B. et al. Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene. Mammalian Genome 6, 658–661 (1995). https://doi.org/10.1007/BF00352375

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