References
Ebersole, T.A., Chen, D., Justice, M.J. & K., Artzt Nature Genet. 12, 260–265 (1996).
Lewis, E.B. Adv. Genet. 3, 73–115 (1950).
Lima-de-Faria, A. In Molecular evolution and organization of the chromosome 531–604 (EIsevier, New YorK 1983).
Henikoff, S. Trends Genetics 6, 422–426 (1990).
Eissenberg, J.C. Bioessays 11, 14–17 (1989).
Clark, S.H. & Chovnick, A. Genet. 114, 819–840 (1986).
Duncan, I. Annu. Rev Genet. 21, 285–319 (1987).
Russell, L.B. & Montgomery, C.S. Genetics 61, 281–312 (1970).
Cattanach, B.M. Gen. Res. Camb. 23, 291–306 (1974).
Lacy, E. et al. Cell 34, 343–358 (1983).
Mintz, B. & Bradl, M. Proc. Natl. Acad. Sci. USA 88, 9643–9647 (1991).
Robertson, G. et al. Proc. Natl. Acad. Sci. USA 92, 5371–5375 (1995).
Potter, M. Carcinogenesis 11, 1–13 (1990).
Magrath, I. Adv. Cancer Res. 55, 133–270 (1990).
Cockerill, P.N. & Garrard, W.T. Cell 44, 273–282 (1986).
Hortnagel, K. et al. Oncogene 10, 1393–1401 (1995).
Bartholomew, C. & Ihle, J.N. Mol. Cell. Biol. 11, 1820–1828 (1991).
Townes, T.M. & Behringer, R.R. Trends Genet. 6, 219–223 (1990).
Romao, L. et al. Blood 78, 1589–1595 (1991).
Stamatoyannopoulos, G. & Nienhuis, A.W. in The Molecular Basis of Blood Diseases 2nd Ed. 107–155 (W.B. Saunders, Philadelphia, 1994).
Fiengold, E.A. & Forget, B.G. Blood 74, 2178–2186 (1989).
Elder, J.T. et al. Mol. Cell. Biol. 10, 1382–1389 (1990).
Duttlinger, R. et al. Development 118, 705–717 (1993).
Bedell, M.A. et al. Genes Dev. 9, 455–470 (1995).
Miller, M.W. et al. EMBO J. 13, 1806–1816 (1994).
Brannan, C.I. et al. Genes Dev. 6, 1832–1842 (1992).
Peters, G.A. J. Cell Science Supplement 18, 89–96 (1994).
Lammie, G.A. et al. Oncogene 7, 2381–2387 (1992).
Morishita, K. et al. Proc. Natl. Acad. Sci. USA 89, 3937–3941 (1992).
Levy, E.R. et al. Blood 83, 1348–1354 (1994).
Suzukawa, K. et al. Blood 84, 2681–2688 (1994).
Hengtein, B. et al. Mol. Cell. Biol. 9, 2105–2113 (1989).
Zeidler, R. et al. Genes Chrom. Cancer. 9, 282–287 (1994).
Axelson, H. et al. Oncogene 6, 2263–2270 (1991).
Shaughnessy, J. et al. Oncogene 9, 247–253 (1994).
Tsichlis, P.N. et al. J. Virol. 64, 2236–2244 (1990).
Tsichlis, R.N. et al. Proc. Natl. Acad. Sci. USA 86, 5487–5491 (1989).
Driscoll, M.C. et al. Proc. Natl. Acad. Sci. USA 86, 7470–7474 (1989).
Fantes, J. et al. Hum. Mol. Genet. 4, 415–422 (1995).
de Kok, Y.J.M. et al. Science 267, 685–688 (1995).
de Kok, Y.J.M. et al. Hum. Mol. Genet. 4, 2145–2150 (1995).
Foster, J.W. et al. Nature. 372, 525–530 (1994).
Kwok, C. et al. Am. J. Hum. Genet. 57, 1028–1036 (1995).
Wagner, T. et al. Cell 79, 1111–1120 (1994).
Cordes, S.R. & Barsh, G.S. Cell 79, 1025–1034 (1994).
Capel, B. et al. Nature Genet. 5, 301–307 (1993).
Laval, S.H. et al. Proc. Natl. Acad. Sci. USA 92, 10403–10407 (1995).
Avraham, K.B. et al. Nature Genet. 11, 369–375 (1995).
Duttlinger, R. et al. Proc. Natl. Acad. Sci. USA 92, 3754–3758 (1995).
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Bedell, M., Jenkins, N. & Copeland, N. Good genes in bad neighbourhoods. Nat Genet 12, 229–232 (1996). https://doi.org/10.1038/ng0396-229
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DOI: https://doi.org/10.1038/ng0396-229
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