• Banfi, S., Borsani, G., Rossi, E., Bernard, L., Guffanti, A., Rubboli, F., Marchitiello, A., Giglio, S., Coluccia, E., Zollo, M., Zuffardi, O., Ballabio, A. (1996). Identification and mapping of human cDNAs homologous toDrosophila mutant genes through EST database searching. Nature Genet. 13, 167–174.

  Article PubMed CAS  Google Scholar 

• Bolcato-Bellemin, A.L., Stoetzel, C, Bourgeois, P., Sobieszczuk, D., Dierich, A., Le Meur, M., Gerlinger, P., Perrin-Schmitt, F. (submitted). Lethal defects in both extra-embryonic and embryonic tissues of murine gastrula lackingM-twist function.

• Garcia-Esquivel, L., Garcia-Cruz, D., Rivera, H., Plascencia, M.L., Cantu, J.M. (1986). De novo del(7)(pter-p21.2::pl5.2-qter) and craniosynostosis: implications for critical segment assignment in the 7p2 monosomy syndrome. Ann. Genet. 29, 36–38.

  PubMed CAS  Google Scholar 

• Hopwood, N.D., Pluck, A., Gurdon, J.B. (1989). AXenopus mRNA related toDrosophila twist is expressed in response to induction in the mesoderm and the neural crest. Cell 59, 893–903.

  Article PubMed CAS  Google Scholar 

• Inglehearn, C., Keen, T.J., Al-Maghteh, M., Bhattacharya, S. (1994). Loci for autosomal dominant retinitis pigmentosa and dominant cystoid macular dystrophy on chromosome 7p are not allelic. (Letter) Am. J. Genet. 55, 581–582.

  CAS  Google Scholar 

• Kremer, H., Pinckers, A., van den Heim, B., Deutman, A.F., Ropers, H.H., Mariman, E.C.M. (1994). Localisation of the gene for dominant cystoid macular dystrophy on chromosome 7p. Hum. Mol. Genet. 3, 299–302.

  Article PubMed CAS  Google Scholar 

• Lyon, M.F., Kirby, M.C. (1995). The mouse chromosome atlas. Mouse Genome. 93, 23–66.

  Google Scholar 

• Mattei, M.G., Philip, N., Passage, E., Moisan, J.P., Mandel, J.L., Mattei, J.F. (1985). DNA probe localization at 18pll3 band byin situ hybridization and identification of a small supernumerary chromosome. Hum. Genet. 69, 268–271.

  Article PubMed CAS  Google Scholar 

• Mattei, M.G., Stoetzel, C., Perrin-Schmitt, F. (1993). The B-HLH protein encodingM-twist gene is located byin situ hybridisation on murine chromosome 12. Mamm. Genome 4, 127–128.

  Article PubMed CAS  Google Scholar 

• Rose, C.S.P., King, A.A.J., Summers, D., Palmer, R., Yang, S., Wilkie, A.O.M., Reardon, W., Malcolm, S., Winter, R.M. (1994). Localization of the genetic locus for Saerthre-Chotzen syndrome to a 6cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2. Hum. Mol. Genet. 3, 1405–1408.

  Article PubMed CAS  Google Scholar 

• Sambrook, J., Fritsch, E.F., Maniatis, T. (1989).Molecular Cloning: A Laboratory Manual, 2nd ed. (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press).

  Google Scholar 

• Sanger, F. (1981). Determination of nucleotide sequences in DNA. Science 214, 1205–1210.

  Article PubMed CAS  Google Scholar 

• Stoetzel, C., Weber, B., Bourgeois, P., Bolcato-Bellemin, A.L., Perrin-Schmitt, F. (1995). Dorso-ventral and rostro-caudal sequential expression ofM-twist in postimplanted murine embryos. Mech. Dev. 51, 251–264.

  Article PubMed CAS  Google Scholar 

• Thisse, B., Stoetzel, C., Gorostiza-Thisse, C., Perrin-Schmitt, F. (1988). Sequence of thetwist gene and nuclear localization of its protein in endomesodermal cells of earlyDrosophila embryos. EMBO J. 77, 2175- 2183.

  Google Scholar 

• Wolf, C., Thisse, C., Stoetzel, C., Thisse, B., Gerlinger, P., Perrin-Schmitt, F. (1991). TheM-twist gene ofMus is expressed in subsets of mesodermal cells and is closely related to theXenopus X-twi andDrosophila twist genes. Dev. Biol. 143, 363–373.

  Article PubMed CAS  Google Scholar 

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