This is a preview of subscription content, log in via an institution to check access.
References
Barbosa, M.D.F.S., Johnson, S.A., Achey, K., Gutierrez, M.J., Wakeland, E.K., Zerial, M., Kingsmore, S.F. (1996). The Rab protein family: genetic mapping of six Rab genes in the mouse. Genomics 30, 439–444.
Brunialti, A.L.B., Poirier, C., Schmalbruch, H., Guénet, J.-L. (1995). The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13. Genomics 29, 131–135.
Collins, F.S. (1995). Positional cloning moves from perditional to traditional. Nature Genet. 9, 347–350.
Dietrich, W.F., Miller, J.C., Steen, R.G., Merchang, M., Damron, D., Nahf, R., Gross, A., Joyce, D.C., Wessel, M., Dredge, R.D., Marquis, A., Stein, L.D., Goodman, N., Page, D.C., Lander, E.S. (1994). A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nature Genet. 7, 220–245.
Durkin, M.E., Chakravarti, S., Bartos, B.B., Liu, S.H., Friedman, R.L., Chung, A.E. (1988). Amino acid sequence and domain structure of entactin. Homology with epidermal growth factor precursor and low density lipoprotein receptor. J. Cell Biol. 107, 2749–2756.
Durkin, M.E., Wewer, U.M., Chung, A.E. (1995). Exon organization of the mouse entactin gene corresponds to the structural domains of the polypeptide and has regional homology to the low-density lipoprotein receptor gene. Genomics 26, 219–228.
Hui, C.C., Joyner, A.L. (1993). A mouse model of Greig cephalopolysyndactyly syndrome: the extra-toesJmutation contains an intragenic deletion of the Gli3 gene. Nature Genet. 3, 241–246.
Hunter, K.W., Watson, M.L., Rochelle, J., Ontiveros, S., Munroe, D., Seidin, M.F., Housman, D.E. (1993). Single-strand conformational polymorphism (SSCP) mapping of the mouse genome: integration of the SSCP, microsatellite, and gene maps of mouse chromosome 1. Genomics 18, 510–519.
Kingsmore, S.F., Watson, M.L., Howard, T.A., Seidin, M.F. (1989). A 6000 kilobase segment of chromosome 1 is conserved in human and mouse. EMBO J. 8, 4073–4080.
Kingsmore, S.F., Barbosa, M.D.F.S., Tchernev, V.T., Detter, J.C., Loosie, A.C., Seidin, M.F., Holcombe, R.F. (1996). Positional cloning of the Chediak-Higashi syndrome gene: Genetic mapping of the beige locus on mouse Chromosome 13. J. Invest. Med., in press.
Kusumi, K., Smith, J.S., Segre, J.A., Koos, D.S., Lander, E.S. (1993). Construction of a large-insert yeast artificial chromosome library of the mouse genome. Mamm. Genome 4, 391–392.
Lane, P.W. (1971). Xt-bg-cr linkage. Mouse News Lett. 45, 29.
Lovett, M. (1994). Fishing for complements: finding genes by direct selection. Trends Genet. 10, 352–357.
Lovett, M., Kere, J., Hinton, L.M. (1991). Direct selection: a method for the isolation of cDNAs encoded by large genomic regions. Proc. Natl. Acad. Sci. USA 88, 9628–9632.
Lyon, M.F., Meredith, R. (1969). Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. Genet. Res. 14, 163–166.
Lyon, M.F., Morris, T., Searle, A.G., Butler, J. (1967). Occurrences and linkage relations of the mutant extra-toes in the mouse. Genet. Res. 9, 383–385.
Nehls, M., Lüno, K., Schorpp, M., Pfeifer, D., Krause, S., Matysiak-Scholze, U., Dierbach, H., Boehm, T. (1995). YAC/P1 contigs defining the location of 56 microsatellite markers and several genes across a 3.4-cM interval on mouse Chromosome 11. Mamm. Genome 6, 321–331.
Pierce, J.C., Sauer, B., Sternberg, N. (1992). A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: improved cloning efficacy. Proc. Natl. Acad. Sci. USA 89, 2056–2060.
Simmler, M.C., Cox, R.D., Avner, P. (1991). Adaptation of the interspersed repetitive sequence polymerase chain reaction to the isolation of mouse DNA probes from somatic cell hybrids on a hamster background. Genomics 10, 770–778.
Swank, R.T., Sweet, H.O., Davisson, M.T., Reddington, M., Novak, E.K. (1991). Sandy: a new mouse model for platelet storage pool deficiency. Genet. Res. 58, 51–62.
Vortkamp, A., Franz, T., Gessler, M., Grzeschik, K.H. (1992). Deletion of GLI3 supports the homology of the human Greig cephalopolysyndactyly syndrome (GCPS) and the mouse mutation extra toes (Xt). Mamm. Genome 3, 461–463.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kingsmore, S.F., Barbosa, M.D.F.S., Nguyen, Q.A. et al. Physical mapping of the beige critical region on mouse Chromosome 13. Mammalian Genome 7, 773–775 (1996). https://doi.org/10.1007/s003359900231
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/s003359900231