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  2. Mammalian Genome
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Comparative map for mice and humans

  • Special Report
  • Published: September 1992
  • Volume 3, pages 480–536, (1992)
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Mammalian Genome Aims and scope Submit manuscript
Comparative map for mice and humans
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  • Joseph H. Nadeau1,
  • Muriel T. Davisson1,
  • Donald P. Doolittle1,
  • Patricia Grant1,
  • Alan L. Hillyard1,
  • Michael R. Kosowsky1 &
  • …
  • Thomas H. Roderick1 

  • 338 Accesses

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References

  1. Abbott, C., Piaggio, G., Ammendola, E., Solomon, S., Povey, F., De Simone, G.V., and Cortese, R.. Mapping of the geneTCF2 coding for the transcription factor LFB3 to human chromosome 17 by polymerase chain reaction.Genomics 8: 165–167, 1990.

    Google Scholar 

  2. Abeliovich, D., Kelsey, G.D., McMahon, C.J., Whitehouse, D., Corney, G., Povey, S., Hopkinson, D.A., Attwood, J., Mieli-Vergani, G., and Mowat, A.P.: Linkage relations of human antichymotrypsin.Cytogenet Cell Genet 46: 567–568, 1987.

    Google Scholar 

  3. Acampora, D., D'Esposito, M., Faiella, A., Pannese, M., Migliaccio, E., Morelli, F., Stornaiulo, A., Nigro, V., Simeone, A., and Boncinelli, E.: The humanHOX gene family.Nucleic Acids Res 17: 10385, 1989.

    Google Scholar 

  4. Acton, R.T., Blankenhorn, E.P., Douglas, T.C., Owen, R.D., Hilgers, J., Hoffman, H.A., and Boyse, E.A.: Variations among sublines of inbred AKR mice.Nature New Biol 245: 8–10, 1973.

    Google Scholar 

  5. Adham, I.M., Grzeschik, K.H., Geurts van Kessel, A.H.M., and Engel, W.: The gene encoding the human preproacrosin (ACR) maps to the q13-qter region on chromosome 22.Hum Genet 84: 59–62, 1989.

    Google Scholar 

  6. Adler, D.A., Tseng, B.Y., Wang, T.S.F., and Disteche, C.M.: Physical mapping of the genes for three components of the mouse DNA replication complex: polymerase a to the X chromosome, primase p49 subunit to chromosome 10, and primase p58 subunit to chromosome 1.Genomics 9:642–646, 1991.

    Google Scholar 

  7. Adolph, S., Bartram, C.R., and Hameister, H.: Mapping of the oncogenesMyc, Sis, andint-1 to the distal part of mouse chromosome 15.Cytogenet Cell Genet 44: 65–68, 1987.

    Google Scholar 

  8. Adolph, S., Berchtold, M.W., and Hameister, H.: Fine localization of genes on distal murine chromosome 15.Cytogenet Cell Genet 52: 177–179, 1989.

    Google Scholar 

  9. Adolph, S., Hameister, H., Zimmer, F.Z., and Zachau, H.G.: TheV(K) genes on human chromosome 22 are located at 22q11.Nucleic Acids Res 16: 6241, 1988.

    Google Scholar 

  10. Adolph, S., Strauss, P.G., and Hameister, H.: Localization of proviral integration sites (Mlvi-1, Mlvi-2, andPvt-1) and the alpha globin pseudogene,Hba-3ps, on murine chromosome 15.Cytogenet Cell Genet 47: 189–191, 1988.

    Google Scholar 

  11. Adolph, S., Strauss, P.G., Hameister, H., and Vogel, W.: Physical gene map of murine chromosome 15.Cytogenet Cell Genet 46: 567–568, 1987.

    Google Scholar 

  12. Adra, C.N., Ellis, N.A., and McBurney, M.W.: The family of mouse phosphoglycerate kinase genes and pseudogenes.Somatic Cell Mol Genet 14: 69–81, 1988.

    Google Scholar 

  13. Affara, N.A., Chambers, D., O'Brien, J., Habeebu, S.S.M., Kalaitsidaki, M., Bishop, C.E., and Ferguson-Smith, M.A.: Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X, Y and 9.Nucleic Acids Res 17: 2987–2999, 1989.

    Google Scholar 

  14. Affholter, J.A., Hsieh, C.L., Francke, U., and Roth, R.A.: Insulin-degrading enzyme: stable expression of the human complementary DNA, characterization of its protein product, and chromosomal mapping of the human and mouse genes.Mol Endocrinol 4: 1125–1135, 1990.

    Google Scholar 

  15. Aitken, D.A. and Ferguson-Smith, M.A.: Intra-chromosomal assignment of the structural gene forGALT to the short arm of chromosome 9 by gene dosage studies.Cytogenet Cell Genet 25: 131, 1979.

    Google Scholar 

  16. Akamizu, T., Ikuyama, S., Saji, M., Kosugi, S., Kozak, C., McBride, O.W., and Kohn, L.D.: Cloning, chromosomal assignment, and regulation off the rat thyrotropin receptor: expression of the gene is regulated by thyrotropin, agents that increase cAMP levels, and thyroid antibodies.Proc Natl Acad Sci USA 87: 5677–5681, 1990.

    Google Scholar 

  17. Akao, Y., Utsumi, K.R., Naito, K., Uea, R., Takahashi, T., and Yamada, K.: Chromosomal assignments of genes coding for human leukocyte common antigen, T-200, and lymphocyte function-associated antigen 1, LFA-1 beta subunit.Somatic Cell Mol Genet 13: 273–278, 1987.

    Google Scholar 

  18. Akao, Y., Utsumi, K.R., Naito, K., Ueda, R., Takahashi, T., and Yamada, K.: Chromosomal assignments of genes coding for T-200 (CD45) and LFA-1 beta (CD18) antigens to human chromosome 1 and 21 respectively.Cytogenet Cell Genet 46: 568, 1987.

    Google Scholar 

  19. Ala-Kapee, M., Forsberg, U.H., Jalkanen, S., and Schroder, J.: Mapping of the gene for human lymphocyte homing receptor to the short arm of human chromosome 11.Cytogenet Cell Genet 51: 948–949, 1989.

    Google Scholar 

  20. Albert, E.D., Baur, M.P., and Mayr, W.R.:Histocompatibility Testing 1984 Springer Verlag, Berlin, 1984.

    Google Scholar 

  21. Allanson, J.E., Gemmill, R.M., Hecht, B.K., Johnsen, S., and Wenger, D.A.: Deletion mapping of the beta-glucuronidase gene.Cytogenet Cell Genet 46: 570, 1987.

    Google Scholar 

  22. Allen, F.M.: Linkage ofML-A andGBG.Vox Sang 27: 382–384, 1974.

    Google Scholar 

  23. Allerdice, P.W., Kaita, H., Lewis, M., McAlpine, P.J., Wong, P., Anderson, J., and Giblett, E.R.: Segregation of marker loci in families with an inherited paracentric insertion of chromosome 9.Am J Hum Genet 39: 612–617, 1986.

    Google Scholar 

  24. Allore, R.J., Hanlon, K.M., Neilson, K.M., Marks, A., and Dunn, R.J.: Cloning and chromosomal localization of the human s100 protein beta subunit gene.Genome 30: 218, 1988.

    Google Scholar 

  25. Allore, R., O'Hanlon, D., Price, R., Neilson, K., Willard, H.F., Cox, D.R., Marks, A., and Dunn, R.J.: Gene encoding the B subunit of S100 protein is on chromosome 21: implications for Down syndrome.Science 239: 1311–1313, 1988.

    Google Scholar 

  26. Alper, C.A.: Inherited structural polymorphism in human C2. Evidence for genetic linkage betweenC2 andBf.J Exp Med 144: 1111–1114, 1976.

    Google Scholar 

  27. Amar, L.C., Dandolo, L., Hanauer, A., Ryder-Cook, A., Arnaud, D., Mandel, J.L., and Avner, P.: Conservation and reorganization of loci on the mammalian X chromosome: a molecular frame work for the identification of homologous subchromosomal regions in man and mouse.Genomics 2: 220–230, 1988.

    Google Scholar 

  28. Amorim, A., Schunter, F., Ritter, H., and Kompf, J.: Linkage studies on the ALAD polymorphism.Cytogenet Cell Genet 37: 400, 1984.

    Google Scholar 

  29. Anagnou, N.P., Antonarakis, S.E., O'Brien, S.J., and Modi, W.S.: Chromosomal localization and racial distribution of the polymorphic human dihydrofolate reductase pseudogene (DHFRPI).Am J Hum Genet 42: 345–352, 1988.

    Google Scholar 

  30. Anagnou, N.P., Economou-Pachnis, A., O'Brien, S.J., Modi, W.S., Nienhuis, A.W., and Tsichlis, P.N.: The human homologue of the Moloney leukemia virus integration 2 locus (MLV12) is on the short arm of chromosome 5.Cytogenet Cell Genet 46: 571, 1987.

    Google Scholar 

  31. Anagnou, N.P., Economou-Pachnis, A., O'Brien, S.J., Modi, W.S., Nienhuis, A.W., and Tsichlis, P.N.: The human homolog of the Moloney leukemia virus integration 2 locus (MLV2) maps to band p14 of chromosome 5.Genomics 5: 354–358, 1989.

    Google Scholar 

  32. Anderson, I.J., Goldberg, R.B., Marion, R.W., Upholt, W.B., and Tsipouras, P.: Spondyloepiphyseal dysplasia congenita: genetic linkage to type II collagen (COL2A1).Am J Hum Genet 46: 896–901, 1990.

    Google Scholar 

  33. Andrews, S.J. and Peters, J.: Linkage analyses and biochemical genetics of sorbitol dehydrogenase-1 (Sdh-1) in the mouse.Biochem Genet 21: 809–817, 1983.

    Google Scholar 

  34. Andria, M.L., Hsieh, C.L., Oren, R., Francke, U., and Levy, S.: Genomic organization and chromosomal localization of theTAPA-1 gene.J Immunol 147: 1030–1036, 1991.

    Google Scholar 

  35. Antonucci, T.K., von Deimling, O.H., Rosenblum, B.B., Skow, L.C., and Meisler, M.H.: Conserved linkage within a 4-cM region of mouse chromosome 9 and human chromosome 11.Genetics 107: 463–475, 1984.

    Google Scholar 

  36. Archer, B.T., Ozcelik, T., Jahn, R., Francke, U., and Sudhof, T.C.: Structures and chromosomal localizations of two human genes encoding synaptobrevins 1 and 2.J Biol Chem 265: 17267–17273, 1990.

    Google Scholar 

  37. Arden, K.C., Boutin, J.M., Djiane, J., Kelly, P.A., and Cavenee, W.K.: The receptors for prolactin and growth hormone are localized in the same region of human chromosome 5.Cytogenet Cell Genet 53: 161–165, 1990.

    Google Scholar 

  38. Arheden, K., Mandahl, N., Strombeck, B., Isaksson, M., and Mitelman, F.: Chromosomal localization of the human oncogeneInt-1 to 12q13 by in situ hybridization.Cytogenet Cell Genet 46: 571, 1987.

    Google Scholar 

  39. Arinami, T., Hirano, T., Kobayashi, K., Yamanouchi, Y., and Hamaguchi, H.: Assignment of the apolipoproteinA-I gene to 11q23 based on RFLP in a case with partial deletion of chromosome 11, del(11) (q23.3-qter).Hum Genet 85: 39–40, 1990.

    Google Scholar 

  40. Ark, B., Gummere, G., Bennett, D., and Artzt, K.: Mapping of thePim-1 oncogene in mouset-haplotypes and its use to define the relative map positions of thetcl loci t〈0〉t〈6〉 and t〈w12〉 and the markertf (tufted).Genomics 10: 385–389, 1991.

    Google Scholar 

  41. Arnemann, J., Spurr, N.K., Wheeler, G.N., Parker, A.E., and Buxton, R.S.: Chromosomal assignment of the human genes coding for the major proteins of the desmosome junction, Desmoglein DGI (DSG), Desmocollins DGII/III (DSC), Desmoplakins DPI/II (DSP), and Plakoglobin DPIII (JUP).Genomics 10: 640–645, 1991.

    Google Scholar 

  42. Artzt, K., Barlow, D., Dove, W.H., Fischer-Lindahl, K., Klein, J., Lyon, M.F., and Silver, L.M.: (Committee for Mouse Chromosome 17). Maps of mouse chromosome 17: first report.Mammalian Genome 1: 5–29, 1991.

    Google Scholar 

  43. Arveiler, B., Vincent, A., and Mandel, J.L.: Toward a physical map of the Xq28 region in man: linking color vision, G6PD and coagulation factor VIII genes to an X-Y homology region.Genomics 4: 460–471, 1989.

    Google Scholar 

  44. Arwert, F., Porck, H.J., Frater-Schroder, M., Brahe, C., Guerts van Kessel, A., Westerveld, A., Meera Khan, P., Zang, K., Frants, R.R., Kortbeek, H.T., and Erikson, A.W.: Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells.Hum Genet 74: 378–381, 1986.

    Google Scholar 

  45. Ashley, P.L. and Cox, D.R.: Further evidence of homology between human chromosome 21 and the distal tip of mouse chromosome 16.Cytogenet Cell Genet 46: 573, 1987.

    Google Scholar 

  46. Ashley, P.L., Ellison, J., Sullivan, K.A., Bourne, H.R., and Cox, D.R.: Chromosomal assignment of the murineGia andGsa genes. Implications for the obese mouse.J Biol Chem 262: 15299–15301, 1987.

    Google Scholar 

  47. Ashley, P.L., Flandermeyer, R.R., and Cox, D.R.: Identification of novel phosphofructokinase loci in mouse and man.Am J Hum Genet 39: A186, 1986.

    Google Scholar 

  48. Ashley, P.L., Price, E.R., Lebo, R.V., and Cox, D.R.: An expressed phosphofructokinase gene (PFKX) maps to human chromosome 12 and mouse chromosome 15.Cytogenet Cell Genet 46: 573, 1987.

    Google Scholar 

  49. Ashworth, A. and Willison, K.: Chromosomal localization of mouse cDNAs homologous to the Drosophila gene kruppel.Mouse News Lett 79: 84, 1987.

    Google Scholar 

  50. Ashworth, A., Williams, B.P., Buchberg, A.M., Goodfellow, P.N., Solomon, E., Potter, J., and Willison, K.R.: Chromosomal localization of zinc finger protein genes in man and mouse.Genomics 4: 323–327, 1989.

    Google Scholar 

  51. Askew, D.S., Bartholomew, C., Buchberg, A.M., Valentine, M.B., Jenkins, N.A., Copeland, N.G., and Ihle, J.N.:His-1 andHis-2: identification and chromosomal mapping of two commonly rearranged sites of viral integration in a myeloid leukemia.Oncogene 6: 2041–2047, 1991.

    Google Scholar 

  52. Aston, C.E., Sherman, S.L., Morton, N.E., Speiser, P.W., and New, M.I.: Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies.Am J Hum Genet 43: 304–310, 1988.

    Google Scholar 

  53. Astrin, K.H. and Bishop, D.F.: Assignment of the human erythroidD-aminolevulinate synthase (ALAS2) to the X chromosome.Cytogenet Cell Genet 51: 953, 1989.

    Google Scholar 

  54. Astrin, K.H., Desnick, R.J., and Smith, M.: Provisional assignment of esterase B3 (ESB3) to human chromosome 16.Cytogenet Cell Genet 32: 250, 1982.

    Google Scholar 

  55. Aula, P., Leisti, J., and von Koskull, H.: Partial trisomy 21.Clin Genet 4: 241–245, 1973.

    Google Scholar 

  56. Avner, P., Amar, L., Arnaud, D., Hanauer, A., and Cambrou, J.: Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecificMus spretus mouse cross.Proc Natl Acad Sci USA 84: 1629–1633, 1987.

    Google Scholar 

  57. Avner, P., Bucan, M., Arnaud, D., Lehrach, H., and Rapp, U.:A-raf oncogene localizes on mouse X chromosome to region some 10–17 centimorgans proximal to hypoxanthine phosphoribosyltransferase gene.Somatic Cell Mol Genet 13: 267–272, 1987.

    Google Scholar 

  58. Azen, E., Carlson, D.M., Lalley P.A., and Vanin, E.: Salivary proline-rich genes on chromosome 8 of mouse.Science 226: 967–969, 1984.

    Google Scholar 

  59. Azen, E., Goodman, P.A., and Lalley, P.A.: Human salivary proline-rich protein genes on chromosome 12.Am J Hum Genet 37: 418–424, 1985.

    Google Scholar 

  60. Azen, E.A., Davisson, M.T., Cherry, M., and Taylor, B.A.:Prp (proline-rich protein) genes linked to markersEs-12 (esterase-12),Ea-10 (erythrocyte alloantigen) and loci on distal mouse chromosome 6.Genomics 5: 415–422, 1989.

    Google Scholar 

  61. Azoulay, M., Henry, I., Tata, F., Weil, D., Grzeschik, K.H., Chaves, M.E., McIntyre, N., Williamson, R., Humphries, S.E., and Junien, C.: The structural gene for lecithin: cholesterol acyl transferase (LCAT) maps to 16q22.Ann Hum Genet 51: 129–136, 1987.

    Google Scholar 

  62. Bach, I., Galcheva-Gargova, Z., Mattei, M.G., Simon-Chazottes, D., Guenet, J.L., Cereghini, S., and Yaniv, M.: Cloning of human hepatic nuclear factor 1 (HNF1) and chromosomal localization of its gene in man and mouse.Genomics 8: 155–164, 1990.

    Google Scholar 

  63. Baecher, C.M., Dorfman, K.S., Mattei, M.G., and Frelinger, J.G.: cDNA cloning and localization of the mouse leukosialin gene (Ly48) to chromosome 7.Immunogenetics 31: 307–314, 1990.

    Google Scholar 

  64. Baker, E., Chen, L.Z., Smith, C.A., Callen, D.F., Goodwin, R., and Sutherland, G.R.: Chromosomal localization of the human tumor necrosis factor receptor genes.Cytogenet Cell Genet 57: 117–118, 1991.

    Google Scholar 

  65. Balazs, I., Neuweiler, J., and Van de Stadt, I.: Genetic linkage studies of six polymorphic loci in chromosome 12 recognized by cDNA clones.Cytogenet Cell Genet 46: 574, 1987.

    Google Scholar 

  66. Bale, A.E., Nebert, D.W., and McBride O.W.: Subchromosomal localization of the dioxin-inducible P1450 locus (CYP1) and description of two RFLPs detected with a 3′P1450 cDNA probe.Cytogenet Cell Genet 46:574–575, 1987.

    Google Scholar 

  67. Bale, S.J., Bale, A.E., Stewart, K., Dachowski, L., McBride, O.W., Glaser, T., Green, J.E., Mulvihill, J.J., Brandi, M.L., Sakaguchi, K., Auerbach, G.D., and Marx, S.J.: Linkage analysis of multiple endocrine neoplasia type 1 withINT2 and other markers on chromosome 11.Genomics 4: 320–322, 1989.

    Google Scholar 

  68. Ball, S.P., Tongue, N., Gibaud, A., LePendu, J., Mollicone, R., Gerard, G., and Oriol, R.: The human chromosome 19 linkage group,FUT1 (H), FUT2 (SE), LE, LU PEPD, C3, APOC2, D19S7 andD19S9.Ann Hum Genet 55: 225–233, 1991.

    Google Scholar 

  69. Ballantyne, C.M., Kozak, C.A., O'Brien, W.E., and Beaudet, A.L.: Assignment of the gene for intercellular adhesion molecule-1 (Icam-1) to proximal mouse chromosome 9.Genomics 9: 547–550, 1991.

    Google Scholar 

  70. Baranov, V.S., Schwartzman, A.L., Gorbunova, V.N., Gaitskhoki, V.S., Rubtsov N.B., and Timchenko, N.A.: Chromosomal localization of ceruplasmin and transferrin genes in laboratory rats, mice and in man by hybridization with specific DNA probes.Chromosoma 96: 60–66, 1987.

    Google Scholar 

  71. Baranov, V.S., Shwartzman, A.L., Gorbunova, V.N., Gaitskhoki, V.S., and Neifakh, S.A.: Mapping of the ceruloplasim gene on human and laboratory mouse chromosomes by direct in situ hybridization.Soviet Genet 21: 315–324, 1985.

    Google Scholar 

  72. Barker, P.E., Rabin, M., Watson M., Breg, W.R., Ruddle, F.H., and Verma, I.M.: Human c-fos oncogene mapped within chromosomal region 14q21-q31.Proc Natl Acad Sci USA 81: 5826–5830, 1984.

    Google Scholar 

  73. Barker, P.E., Royer, H.D., Ruddle, F.H., and Reinherz, E.L.: Human T cell receptor geneTCRA lies in region 14pter-q21.Cytogenet Cell Genet 40: 576–577, 1985.

    Google Scholar 

  74. Barker, P.E., Ruddle, F.H., Royer, H.D., Acuto, O., and Reinherz, E.L.: Chromosomal location of human T-cell receptor geneTib.Science 23: 348–349, 1984.

    Google Scholar 

  75. Barlow, D.P., Bucan, M., Lehrach, H., Hogan, B.L.M., and Gough, N.M.: Close genetic and physical linkage between the murine haemopoietic growth factor genesGM-CSF and multiCSF (IL3).EMBO J 6: 617–623, 1987.

    Google Scholar 

  76. Barnard, P.J., Derry, J.M.J., Ryder-Cook, A.S., and Barnard, E.A.: Localization of the GABA-A receptor alpha-3 subunit gene on the mouse X chromosome.Cytogenet Cell Genet (abstract)51: 958, 1989.

    Google Scholar 

  77. Barnard, P.J., Derry, J.M.J., Ryder-Cook, A.S., Zander, N.F., and Kilimann, M.W.: Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.Cytogenet Cell Genet 53: 91–94, 1990.

    Google Scholar 

  78. Barsh, G.S. and Epstein, C.J.: The long-range restriction map surrounding the mouse agouti locus reveals a disparity between physical and genetic distances.Genomics 5: 9–18, 1989.

    Google Scholar 

  79. Barton, D.E., Arquint, M., Roder, J., Dunn, R., and Francke, U.: The myelin-associated glycoprotein (GMA) maps to human chromosome 19 and mouse chromosome 7.Cytogenet Cell Genet 46: 577, 1987.

    Google Scholar 

  80. Barton, D.E., Arquint, M., Roder, J., Dunn, R., and Francke, U.: The myelin-associated glycoprotein gene: mapping to human chromosome 19 and mouse chromosome 7 and expression in quivering mice.Genomics 1: 107–112, 1987.

    Google Scholar 

  81. Barton, P.R.J., Cohen, A., Robert, B., Fiszman, M.Y., Bonhomme, F., Guenet, J.L., Leader, D.P., and Buckingham, M.E.: The myosin alkali light chains of mouse ventricular and slow skeletal muscle are indistinguishable and are encoded by the same gene.J Biol Chem 260: 8578–8584, 1985.

    Google Scholar 

  82. Barton, D.E., Crimaudo, C., Hortsch, M., and Francke, U.: The genes for ribophorins I and II are on human chromosomes 3q and 20 and mouse chromosomes 6 and 2, respectively.Cytogenet Cell Genet 46: 577, 1987.

    Google Scholar 

  83. Barton, D.E., Foellmer, B.E., Du, J., Tamm, J., Derynck, R., and Francke, U.: Chromosomal mapping of genes for transforming growth factors beta2 and beta3 in man and mouse: dispersion of Tgf-beta gene family.Oncogene Res 3: 323–331, 1988.

    Google Scholar 

  84. Barton, D.E., Foellmer, B.E., Wood, W.I., and Francke, U.: Chromosome mapping of the growth hormone receptor gene in man and mouse.Cytogenet Cell Genet 50: 137–141, 1989.

    Google Scholar 

  85. Barton, D.E., Kwon, B.S., and Francke, U.: Human tyrosinase gene, mapped to chromosome 11 (q14–q21), defines second region of homology with mouse chromosome 7.Genomics 3: 17–24, 1988.

    Google Scholar 

  86. Barton, D.E., Spritz, R.A., and Francke, U.: RPU1 encoding the 68kDa U1 snRNP-associated protein is located on chromosome 19.Cytogenet Cell Genet 46: 577, 1987.

    Google Scholar 

  87. Barton, D.E., Staunton, D., and Francke, U.: The geneBLAST1, encoding a B-cell activation marker, is located on chromosome 1, region cen-q32.Cytogenet Cell Genet 46: 577, 1987.

    Google Scholar 

  88. Barton, D.E., Yang-Feng, T.L., and Francke, U.: The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22-q24) mapped by somatic cell hybrid analysis and in situ hybridization.Hum Genet 72: 221–224, 1986.

    Google Scholar 

  89. Barton, D.E., Yang-Feng, T.L., Mason, A.J., Seeburg, P.H., and Francke, U.:INHA, INHBA, andINHBB, the loci for three subunits of inhibin, mapped in mouse and man.Cytogenet Cell Genet 46: 578, 1986.

    Google Scholar 

  90. Barton, D.E., Yang-Feng, T.L., Mason, A.J., Seeburg, P.H., and Francke, U.: Mapping of genes for inhibin subunits alpha, beta-A, and beta-B on human and mouse chromosomes and studies of jsd mice.Genomics 5: 91–99, 1989.

    Google Scholar 

  91. Barton, D.E., Yang-Feng, T.L., Leto, T., Marchesi, V., and Francke, U.: NEAS encoding a non-erthyroid alpha-spectrin is on chromosome 9, region q33–q34 and on mouse chromosome 2.Cytogenet Cell Genet 46: 578, 1987.

    Google Scholar 

  92. Bartram, C.R., De Klein, A., Hagemeijeri, A., Grosveld, G., and Bootsma, D.: Oncogene translocation in chronic myelocytic leukemia.Cytogenet Cell Genet 37: 415, 1984.

    Google Scholar 

  93. Bartram, C.R., Klein, A., Hagemeijer A., Grosveld, G., Heisterkamp, N., and Groffen, J.: Localization of the human c-sis oncogene in Phl-positive and Phl-negative chronic myelocytic leukemia by in situ hybridization.Blood 63: 223–225, 1984.

    Google Scholar 

  94. Bastian, H., Gruss, P., Duboule, D., and Izpisua-Belmonte, J.C.: The murine even-skipped like geneEvx-2 is closely linked to theHox-4 complex, but is transcribed in the opposite direction.Mammalian Genome 3: 241–243, 1992.

    Google Scholar 

  95. Baumann, H. and Berger, F.G.: Genetic analysis of the major acute phase reactants in the mouse: chromosomal location of the structural genes for haptoglobin and alpha-1-acid glycoprotein-2.Mouse News Lett 71: 49, 1984.

    Google Scholar 

  96. Baumann, H. and Berger, F.G.: Genetics and evolution of the acute phase proteins in mice.Mol Gen Genet 201: 505–512, 1985.

    Google Scholar 

  97. Baumann, H., Held W.A., and Berger, F.G.: The acute phase response of mouse liver: genetic analysis of the major acute phase reactants.J Biol Chem 259: 566–573, 1984.

    Google Scholar 

  98. Beaumont, C., Foubert, C., Grandchamp, B., Weil, D., N'Guyen, V.D., Gross, M.S., and Nordman, Y.: Assignment of the human gene for delta aminolevulinate dehydrase to chromosome 9 by somatic cell hybridization and specific enzyme immunoassay.Ann Hum Genet 48: 153–159, 1984.

    Google Scholar 

  99. Beechey, C., Tweedie, S., Spurr, N., Ball, S., Peters, J., and Edwards, Y.: Mapping of mouse carbonic anhydrase-3,Car-3: another locus in the homologous region of mouse chromosome 3 and human chromosome 8.Genomics 6: 692–696, 1990.

    Google Scholar 

  100. Beeson, D., Jeremiah, S.J., West, L.F., Povey, S., and Newsom-Davis, J.: Assignment of the human acetylcholine receptor b subunit gene to chromosome 17 and the a and d subunit genes to chromosome 2.Cytogenet Cell Genet 51: 960, 1989.

    Google Scholar 

  101. Begley, C.G., Aplan, P.D., Davey, M.P., Nakahara, K., Tchorz, K., Kurtzberg, J., Hershfield, M.S., Haynes, B.F., Cohen, D.I., Waldmann, T.A., and Kirsch, I.R.: Chromosomal translocation in a human leukemic stem-cell line disrupts the T-cell antigen receptor d-chain diversity region and results in a previously unreported fusion transcript.Proc Natl Acad Sci USA 86: 2031–2035, 1989.

    Google Scholar 

  102. Begley, C.G., Visvader, J., Green, A.R., Aplan, P.D., Metcalf, D., Kirsch, I.R., and Gough, N.M.: Molecular cloning and chromosomal localization of the murine homolog of the human helix-loop-helix geneSCL.Proc Natl Acad Sci USA 88: 869–873, 1991.

    Google Scholar 

  103. Bello, M.J., Salagnon, N., Rey, J.A., Guichaoua, M.R., Berge-Lefranc, J.L., Jordan, B.R., and Luciani, J.M.: Precise in situ localization of NCAM, ETS1, and D11S29 on human meiotic chromosomes.Cytogenet Cell Genet 52: 7–10, 1989.

    Google Scholar 

  104. Benchimol, S., Lamb, P., Crawford, L., Sheer, D., Solomon, E., Shows, T., Bruns, G., and Peacock, J.: Humanp53 is on the short arm of chromosome 17.Cytogenet Cell Genet 40: 580–581, 1985.

    Google Scholar 

  105. Bender, K., Bissbort, S., Crone, H., Senff, H., Steiert, A., Neumann, H., Koch, M., Nagel, M., and Wienker, T.F.: Linkage relations ofJK, CO, KEL andIGK with each other and withAHCY1.Hum Hered 38: 12–17, 1988.

    Google Scholar 

  106. Bender, K. and Grzeschik, K.H.: Possible assignment of glyoxalase I (GLO) to chromosome 6 using man-mouse somatic cell hybrids.Hum Genet 61: 127–134, 1982.

    Google Scholar 

  107. Benham, F.J. and Povey, S.: Members of the human glyceraldehyde-3-phosphate dehydrogenase-related gene family map to dispersed chromosomal locations.Genomics 5: 209–214, 1989.

    Google Scholar 

  108. Benham, F.J., Spurr, N., Povey, S., Brinton, B.T., Goodfellow, P.N., Solomon, E., and Harris, T.J.R.: Assignment of tissue-type plasminogen activator to chromosome 8 in man and identification of a common restriction length polymorphism within the gene.Mol Biol Med 2: 251–259, 1984.

    Google Scholar 

  109. Benn, P., Chern, C.J., Bruns, G., Craig, I.W., and Croce, C.M.: Assignment of the genes for human beta-glucuronidase and mitochondrial malate dehydrogenase to the region pter-q22 of chromosome 7.Cytogenet Cell Genet 19: 273–280, 1977.

    Google Scholar 

  110. Berchtold, M.W., Epstein, P., Beaudet, A.L., Payne, M.E., Heizmann, C.W., and Means, A.R.: Structural organization and chromosomal assignment of the parvalbumin gene.J Biol chem 262: 8696–8701, 1987.

    Google Scholar 

  111. Berg, K.: Close linkage between APOB and ACP1 excluded.Cytogenet Cell Genet 46: 580, 1987.

    Google Scholar 

  112. Berge-Lefranc, J.L., Cartouzou, G., Mattei, M.G., Passage, E., Malezet-Desmoulins, C., and Lissitzky, S.: Localization of the thyroglobulin gene by in situ hybridization to human chromosomes.Hum Genet 69: 28–31, 1985.

    Google Scholar 

  113. Berger, F.G. and Paigen, K.:Cis-active control of mouse beta-galactosidase biosynthesis by a systemic regulatory locus.Nature 282: 314–316, 1979.

    Google Scholar 

  114. Bernardi, F., Patracchini, P., Monticelli, A., Varrone, S., Aiello, V., Calzolari, E., Marchetti, G., and Avvedimento, V.E.: Human thyroglobulin gene is located on the terminal part of the long arm of chromosome 8.Cytogenet Cell Genet 40: 582–583, 1985.

    Google Scholar 

  115. Bernier, L., Colman, D.R., and D'Eustachio, P.: Chromosomal locations of genes encoding 2′,3′ cyclic nucleotide 3′-phosphodiesterase and glial fibrillary acidic protein in the mouse.J Neurosci Res 20: 497–504, 1988.

    Google Scholar 

  116. Berube, D., Seralini, G.E., Gagne, R., and Hammond, G.L.: Localization of the human sex hormone-binding globulin gene (SHBG) to the short arm of chromosome 17 (17p12–p13).Cytogenet Cell Genet, 54: 65–67, 1990.

    Google Scholar 

  117. Bhattacharya, S.S., Ludlam, C.A., Clayton, J.F., Strain, L., and Watson, H.: Haemophilia A,F8C, DXS15 andDXS52: establishment of order and evidence for a familial predisposition to crossover.Cytogenet Cell Genet 46: 580, 1987.

    Google Scholar 

  118. Bibbins, K.B., Tsai, J.Y., Schimenti, J., Sarvetnick, N., Zoghbi, H.Y., Goodfellow, P., and Silver, L.M.: Human homologs of two testes-expressed loci on mouse chromosome 17 map to opposite arms of chromosome 6.Genomics 5: 139–143; 1989.

    Google Scholar 

  119. Biddle, F. G. and Petras, M.L.: The inheritance of a nonhemoglobin erythrocytic protein inMus musculus.Genetics 57: 943–949, 1967.

    Google Scholar 

  120. Birkenmeier C.S., McFarland-Starr, E.C., and Barker, J.E.: Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.Proc Natl Acad Sci USA 85: 8121–8125, 1988.

    Google Scholar 

  121. Bishop, D.F., Henderson, A.S., and Astrin, K.H.: HumanD-aminolevulinate synthase: assignment of the housekeeping gene to 3p21 and the erythroid-specific gene to the X chromosome.Genomics 7: 207–214, 1990.

    Google Scholar 

  122. Bissbort, S., Bender, K., and Grzeschik, K.H.: Assignment of the human gene for gamma-glutamyl-cyclotransferase (GCTG) to chromosome 7p.Cytogenet Cell Genet 37: 421, 1984.

    Google Scholar 

  123. Bissbort, S., Hitzeroth, H.W., van den Berg, C.T., and Wienker, T.F.: Linkage relationship between the genes for adenosine deaminase and S-adenosyl-homocysteine hydrolase on human chromosome 20.Hum Genet 77: 277–279, 1987.

    Google Scholar 

  124. Bissbort, S., Hitzeroth, H.W., du Wentzel, D.P., van den Berg, C.W., Senff, H., Wienker, T.F., and Bender, K.: Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14.Hum Genet 79: 289–290, 1988.

    Google Scholar 

  125. Blanche, H., Massart C., Dausset, J., and Cann, H.:TCP1 is not linked toHLA, GLO1, PGK1P2 and other markers in a 45cM map of the short arm of chromosome 6 (6p).Cytogenet Cell Genet 46: 581–582, 1987.

    Google Scholar 

  126. Blanche, H., Zunec, R., Leach, R., Cohen, D., Dausset, J., White, R., and Cann, H.: A 6 point linkage map of the short arm of chromosome 6.Cytogenet Cell Genet 46: 582, 1987.

    Google Scholar 

  127. Blanquet, V., Goldgaber, D., Turleau, C., Creau-Goldberg, N., Delabar, J., Sinet, P.M., Roudier, M., and de Grouchy, J.: The beta amyloid AD-AP cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1.Ann Genet 30: 68–69, 1987.

    Google Scholar 

  128. Blanquet, V., Goldgaber, D., Turleau, C., Creau-Goldberg, N., Delabar, J., Sinet, P.M., Roudier, M., and de Grouchy, J.: In situ hybridization of the b-amyloid protein (APP) cDNA to the vicinity of the interface of 21q21 and q22 in normal and Alzheimer's disease individuals.Cytogenet Cell Genet 46: 582, 1987.

    Google Scholar 

  129. Blanquet, V., Turleau, C., De Grouchy, J., and Creau-Goldberg, N.: Physical mapping around the retinoblastoma gene: possible genomic imprinting suggested by NruI digestion.Genomics 10: 350–355, 1991.

    Google Scholar 

  130. Blatt, C., Eversole-Cire, P., Cohn, V.H., Zollman, S., Fournier, R.E.K., Mohandas, L.T., Nesbitt, M., Lugo, T., Jones, D.T., Reed, R.R., Weiner, L.P., Sparkes, R.S., and Simon, M.I.: Chromosomal localization of genes encoding guanine nucleotide-binding protein subunits in mouse and human.Proc Natl Acad Sci USA 85: 7642–7646, 1988.

    Google Scholar 

  131. Blatt, C., Harper, M.E., Franchini, G., Nesbitt, M.N., and Simon, M.I.: Chromosomal mapping of murine c-fes and c-src genes.Mol Cell Biol 4: 978–981, 1984.

    Google Scholar 

  132. Blatt, C., Saxe, D., Marzluff, W.F., Lobo, S., Nesbitt, M.N., and Simon, M.I.: Mapping and gene order of U1 small nuclear RNA, endogenous viralenv sequence, amylase, and alcohol dehydrogenase-3 on mouse chromosome 3.Somatic Cell Mol Genet 14: 133–142, 1988.

    Google Scholar 

  133. Board, P.G. and Webb, G.C.: Isolation of a cDNA clone and localization of human gluthathione S-transferase 2 genes to chromosome band 6p12.Proc Natl Acad Sci USA 84: 2377–2381, 1987.

    Google Scholar 

  134. Board, P.G., Webb, G.C., and Coggan, M.: Isolation of a cDNA clone and localization of the human glutathione S-transferase 3 genes to chromosome bands 11q13 and 12q13–14.Ann Hum Genet 53: 205–213, 1989.

    Google Scholar 

  135. Bocian, M., Mohandas, T. Sparkes, R.S., and Funderbunk, S.: Peptidase S (PEPS) and phosphoglucomutase 2 (PGM) loci on the short arm of human chromosome 4.Cytogenet Cell Genet 25: 138, 1979.

    Google Scholar 

  136. Bode, V.C., McDonald, J.D., Guénet, J.-L., and Simon, D.:hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosurea mutagenesis.Genetics 118: 299–305, 1988.

    Google Scholar 

  137. Bonhomme, F., Bemehdi, F., Britton-Davidian, J., and Martin, S.: Analyse genetique de croisements interspecifiquesMus musculus L. xMus spretus Lataste: liaison deAdh-1 avecAmy-1 sur le chromosome 3 et deEs-14 avecMod-1 sur le chromosome 9.C R Seances Acad Sci (III) 289: 545–548, 1979.

    Google Scholar 

  138. Bonner, T., O'Brien, S.J., Nash, W.G., Rapp, U.R., Morton, C.C., and Leder P.: Two human homologs of theraf (mil) oncogene are located on human chromosomes 3 and 4.Science 223: 71–74, 1984.

    Google Scholar 

  139. Boultwood J., Breckon, G., Birch, D., and Cox, R.: Chromosomal localization of murine interleukin-1 a and b genes.Genomics 5: 481–485, 1989.

    Google Scholar 

  140. Bowcock, A.M., Crandall, J., Daneshvar, L., Lee, G.M., Young, B., Zunzunegui, V., Craik, C., Cavalli-Sforza, C.L., and King, M.C.: Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families.Am J Hum Genet 39: 699–706, 1986.

    Google Scholar 

  141. Bowcock, A.M., Farrer, L.A., Hebert, J.M., Agger, M., Sternlieb, I., Scheinberg, I.H., Buys, C.H.C.M., Scheffer, H., Frydman, M., Chajek-Saul, T., and Bonne-Tamir, B.: Eight closely linked loci place the Wilson disease locus within 13q14-q21.Am J Hum Genet 43: 664–674, 1988.

    Google Scholar 

  142. Bowcock, A.M., Farrer, L.A., Cavalli-Sforza, L.L., Hebert, J.M., Kidd, K.K., Frydman, M. and Bonne-Tamir, B.: Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.Am J Hum Genet 41: 27–35, 1987.

    Google Scholar 

  143. Bowcock, A.M., Farrer, L.A., Hebert, J.M., Kidd, J.R., Lee, W.H., Kidd, K.K., and Cavalli Sforza, L.L.: Refining the chromosome 13q14 map.Cytogenet Cell Genet 46: 585, 1987.

    Google Scholar 

  144. Bowcock, A.M., Farrer, L.A., Hebert, J.M., Agger, M., Sternleib, I., Frydman, M., Chajek-Saul, T., Lobner, J., Bonne-Tamir, B., and Cavalli-Sforza, L.L.: Several DNA markers tightly linked to Wilson's disease provide evidence against genetic heterogeneity.Am J Hum Genet 43: A138, 1988.

    Google Scholar 

  145. Bowcock, A.M., Kavathas, P., Margolskee, R.F., Herzenberg, L., and Cavalli-Sforza, L.L.: An RFLP associated with pcLeu2-14, a human T-cell differentiation antigen CD8 (Leu2) cDNA mapped to 2p12.Nucleic Acids Res 14: 7817, 1986.

    Google Scholar 

  146. Bowes, C., Li, T., Danciger, M., Baxter, L.C., Appleury, M.L., and Farber, D.B.: Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod receptor cGMP-phosphodiesterase.Nature 347: 677–680, 1990.

    Google Scholar 

  147. Boyd, Y., Craig, I.W., Munro, E., and Migeon, B.R.: Localization of the factor IX locus to Xq26-qter.Cytogenet Cell Genet 37: 425–426, 1984.

    Google Scholar 

  148. Bray, P.F., Barsh, G., Rosa, J.P., Luo, X.Y., Magenis, E., and Shuman, M.A.: Physical linkage and orientation of the genes for platelet membrane glycoproteins GPIIb and GPIIa.Am J Hum Genet 43: A138, 1988.

    Google Scholar 

  149. Brebner, D., Grobler-Rabie, A., Bester, A., Mathew, C., and Boyd, C.: Two new polymorphic markers in the human proa2 (1) collagen gene.Hum Genet 70: 25–27, 1985.

    Google Scholar 

  150. Breen, G.A., Lusis, A.J., and Paigen, K.: Linkage of genetic determinants for mouse beta-galactosidase electrophoresis and activity.Genetics 85: 73–84, 1977.

    Google Scholar 

  151. Brilliant, M.H., Niemann, M.N., and Eicher, E.M.: Murine tyrosine hydroxylase maps to the distal end of chromosome 7 within a region conserved in mouse and man.J Neurogenet 4: 259–266, 1987.

    Google Scholar 

  152. Brilliant, M., Szabo, G., Katarova, Z., Kozak, C.A., Glaser, T.M., Greenspan, R.J., and Housman, D.E.: Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10.Genomics 6: 115–122, 1990.

    Google Scholar 

  153. Brissenden, J.E., Caras, I., Thelander, L., and Francke, U.: The structural gene for the M1 subunit of ribonucleotide reductase maps to chromosome 11, band p15, in human and to chromosome 7 in mouse.Exp Cell Res 174: 302–308, 1988.

    Google Scholar 

  154. Brissenden, J.E., Ullrich, A., and Francke, U.: Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor.Nature 310: 781–784, 1984.

    Google Scholar 

  155. Britton-Davidian, J. and Pasteur, J.: Linkage data in chromosome 7.Mouse News Lett 68: 79, 1983.

    Google Scholar 

  156. Britton-Davidian, J., Ruiz Bustos, A., and Topal, M.: Lactate dehydrogenase polymorphism inMus musculus L. andMus spretus Latase.Experientia 34: 1144–1145, 1978.

    Google Scholar 

  157. Brocas, H., Szpirer, J., Lebo, R.V., Levan, G., Szpirer, C., Cheung, M.C., and Vassart, G.: The thyroglobulin gene resides on chromosome 8 in man and on chromosome 7 in the rat.Cytogenet Cell Genet 39: 150–153, 1985.

    Google Scholar 

  158. Brockdorff, N., Fisher, E.M.C., Orkin, S.H., Lyon, M.F., and Brown, S.D.M.: Localization of the human X-linked gene for chronic granulomatous disease to the mouse X chromosome: implications for X-chromosome evolution.Cytogenet Cell Genet 48: 124–125, 1988.

    Google Scholar 

  159. Brockdroff, N., Amar, L.C., and Brown, S.D.M.: Pulse-field linkage of theP3, G6pd andCf-8 genes on the mouse X chromosome: demonstration of synteny at the physical level.Nucleic Acids Res 17: 1315–1326, 1989.

    Google Scholar 

  160. Brook, J.D., Shaw, D.J., Meredith, L., Bruns, G.A.P., and Harper, P.D.: Localization of genetic markers and orientation of the linkage group on chromosome 19.Hum Genet 68: 282–285, 1984.

    Google Scholar 

  161. Brook, J.D., Skinner, M., Roberts, S.H., Rettig, W.J., Almond, W., and Shaw, D.J.: Further mapping of markers around the centromere of human chromosome 19.Genomics 1: 320–328, 1987.

    Google Scholar 

  162. Brooks, B., Johnson, B., Heinzmann, C., Mohandas, T., Sparkes, R., Jones, S., Bennett, P., Balacs, T., Moore, G., Conley, L., and Hankinson, O.: Localization of a gene required for the nuclear translocation of the dioxin receptor to human chromosome 1 and mouse chromosome 3 and a human RFLP withMspI.Am J Hum Genet (Suppl) 45: A132, 1989.

    Google Scholar 

  163. Brooks, B.A., McBride, O.W., Dolphin, C.T., Farrall, M., Scambler, P.J., Gonzalez, F.J., and Idle, J.R.: The geneCYP3 encodingP450PCN1 (nifedipine oxidase) is tightly linked to the geneCOL1A2 encoding collagen type 1 alpha on 7q21-q22.1.Am J Hum Genet 43: 280–284, 1988.

    Google Scholar 

  164. Brown, C.J., Goss, S.J., Lubahn, D.B., Joseph, D.R., Wilson, E.M., French, F.S., and Willard, H.F.: Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.Am J Hum Genet 4: 264–269, 1989.

    Google Scholar 

  165. Brown, G., Joshua, D.E., Bastin, J., Mason, D.Y., and Barnstable, C.J.: Monoclonal antibodies to human cell surface antigens.Proc Mod Trends Hum Leuk III: 365–368, 1979.

    Google Scholar 

  166. Brown, M.H., Gorman, P.A., Sewall, A., Spurr, N.G., Sheer, D., and Crumpton, M.J.: The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1p.Hum Genet 76: 191–195, 1987.

    Google Scholar 

  167. Brown, R.M., Dahl, H.H.M., and Brown, G.K.: An homologous locus to the human X-linked pyruvate dehydrogenaseE1 alpha subunit gene is located at the distal end of the mouse X chromosome.Cytogenet Cell Genet (Abstr) 51: 970, 1989.

    Google Scholar 

  168. Brown, R.M., Dahl, H.H.M., and Brown, G.K.: Regional localization of the X-linked human pyruvate dehydrogenaseE1a subunit gene.Cytogenet Cell Genet 51: 970, 1989.

    Google Scholar 

  169. Brown, R.M., Dahl, H.H.M., and Brown, G.K.: X-chromosome localization of the functional gene for theE1 alpha subunit of the human pyruvate dehydrogenase complex.Genomics 4: 174–181, 1989.

    Google Scholar 

  170. Brown, S., Lalley, P.A., and Minna, J.D.: Assignment of the gene for peptidase S (PEPS) to chromosome 4 in man and confirmation of peptidase D (PEPD) assignment to chromosome 19.Cytogenet Cell Genet 22: 167–171, 1978.

    Google Scholar 

  171. Brownell, E., Kozak, C.A., Fowle, J.R., Modi, W.S., Rice, N.R., and O'Brien, S.J.: Comparative genetic mapping of cellularrel sequences in man, mouse, and the domestic cat.Am J Hum Genet 39: 194–202, 1986.

    Google Scholar 

  172. Brownell, E., Lee, A.S., Pekar, S.K., Pravtcheva, D., Ruddle, F.H., and Bayney, R.M.: Glial fibrillary protein, an astrocytic-specific marker, maps to human chromosome 17.Genomics 10: 1087–1089, 1991.

    Google Scholar 

  173. Brownell, E., Nash, W., Rice, N., and O'Brien, S.J.: Isolation and chromosomal localization of human cellularREL sequences.Cytogenet Cell Genet 40: 591, 1985.

    Google Scholar 

  174. Brueton, L., Huson, S.M., Winter, R.M., and Williamson, R.: Chromosomal localization of a developmental gene in man: direct DNA analysis demonstrates that Greig Cephalopolysyndactyly maps to 7p13.Am J Med Genet 31: 799–804, 1988.

    Google Scholar 

  175. Brunet, J.F., Denizot, F., Luciani, M.F., Roux-Dosseto, M., Suzan, M., Mattei, M.G., and Golstein, P.: A new member of the immunoglobulin superfamily—CTLA-4.Nature 328: 267–270, 1987.

    Google Scholar 

  176. Brunner, H.G., Smeets, H., Lambermon, H.M.M., Coerwinkel-Driessen, M., van Oost, B.A., Wieringa, B., and Ropers, H.H.: A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.Genomics 5: 589–595, 1989.

    Google Scholar 

  177. Bruns, G.A.P., Eiseman, R.E., and Gerald, P.S.: Human mitochondrial NADP-dependent isocitrate dehydrogenase in man-mouse somatic cell hybrids.Cytogenet Cell Genet 17: 200–211, 1976.

    Google Scholar 

  178. Bruns, G., Gerald, P.S., Lalley, P., Francke, U., and Minna, J.: Gene mapping of the mouse by somatic cell hybridization.Cytogenet Cell Genet 25: 139, 1979.

    Google Scholar 

  179. Bruns, G. and Gerald, P.S.: Human glyceraldehyde-3-phosphate dehydrogenase in man-rodent somatic cell hybrids.Science 192: 54–56, 1976.

    Google Scholar 

  180. Bruns, G.A.P., Leary, A.C., Eisenman, R.E., Bazinet, C.W., Regina, V.M., and Gerald, P.S.: Expression of ACONs and GALT in man-rodent somatic cell hybrids.Cytogenet Cell Genet 22: 172–176, 1978.

    Google Scholar 

  181. Bruns, G.A.P., Leary, A.C., Regina, V.M., and Gerald, P.S.: Lysosomal beta-D-galactosidase in man-hamster somatic cell hybrids.Human Gene Map 4: 177–181, 1977.

    Google Scholar 

  182. Bucan, M., Yang-Feng, T., Colberg-Poley, A.M., Wolgemuth, D.J., Guenet, J.L., Francke, U., and Lehrach, H.: Genetic and cytogenetic localization of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.EMBO J 5: 2899–2905, 1986.

    Google Scholar 

  183. Buchberg, A.M., Bedigian, H.G., Taylor, B.A., Brownell, E., Ihle, J.N., Nagata, S., Jenkins, N.A., and Copeland, N.G.: Localization ofEvi-2 to chromosome 11: linkage to other proto-oncogenes and growth factor loci using interspecific backcross mice.Oncogene Res 2: 149–165, 1988.

    Google Scholar 

  184. Buchberg, A.M., Brownell, E., Nagata, S., Jenkins, N.A., and Copeland, N.G.: A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and human.Genetics 122: 153–161, 1989.

    Google Scholar 

  185. Buchberg, A.M., Jenkins, N.A., and Copeland, N.G.: Localization of the murine macrophage colony-stimulating factor gene to chromosome 3 using interspecific backcross analysis.Genomics 5: 363–367, 1989.

    Google Scholar 

  186. Buckle, V.J., Fujita, N., Bateson, A.N., Darlison, M.G., and Barnard, E.A.: Localization of the humanGABA-A3 receptor subunit gene to Xq28: a candidate gene for X-linked manic depression.Cytogenet Cell Genet 51: 972, 1989.

    Google Scholar 

  187. Buckle, V.J., Guénet, J.-L., Simon-Chazottes, D., Lowe, D.R., and Davies, K.E.: Localization of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.Hum Genet 85: 324–326, 1990.

    Google Scholar 

  188. Buckwalter, M.S., Katz, R.W., and Camper, S.A.: Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an interspecific backcross.Genomics 10: 515–526, 1991.

    Google Scholar 

  189. Budarf, M., Canaani, E., and Emanuel, B.S.: Linear order of the fourBCR-related loci in 22q11.Genomics 3: 168–171, 1988.

    Google Scholar 

  190. Budarf, M., Emanuel, B.S., Mohandas, T., Goeddel, D.V., and Lowe, D.G.: Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint 22q.Cytogenet Cell Genet 52: 19–22, 1989.

    Google Scholar 

  191. Budarf, M., Huebner, K., Emanuel, B., Croce, C.M., Copeland, N.G., Jenkins, N.A., and D'Andrea, A.D.D.: Assignment of the erythropoietin receptor (EPOR) gene to mouse chromosome 9 and human chromosome 19.Genomics 8: 575–578, 1990.

    Google Scholar 

  192. Buetow, K.H., Murray, J.C., DeHayen, C.R., Ardinger, R.H., Weiss, M.L., and Nemer, M.: Linkage analysis of seven markers on human chromosome 1.Cytogenet Cell Genet 46: 588, 1987.

    Google Scholar 

  193. Buetow, K.H., Nishimura, D., Green, P., Nakamura, Y., Jiang, O., and Murray, J.C.: A detailed multipoint gene map of chromosome 1q.Genomics 8: 13–21, 1990.

    Google Scholar 

  194. Buetow, K.H., Nishimura, D., Green, P., Nakamura, Y., Jiang, O., and Murray, J.C.: A detailed multipoint gene map of chromosome 1q.Genomics 8: 13–21, 1990.

    Google Scholar 

  195. Bulfield, G.: Genetics of atherosclerosis and plasma lipoproteins in mice.Trends Genet 4: 3–4, 1988.

    Google Scholar 

  196. Bulfield, G., Siller, W.G., Wright, P.A.L., and Moore, K.J.: X chromosome-linked muscular dystrophy (mdx) in the mouse.Proc Natl Acad Sci USA 81: 1189–1192, 1984.

    Google Scholar 

  197. Bullard, D.C. and Schimenti, J.C.: Molecular cloning and genetic mapping of thet complex responder candidate gene family.Genetics 124: 957–966, 1990.

    Google Scholar 

  198. Burgess, A.W., Lloyd, C.J., and Nice, E.C.: Murine epidermal growth factor: heterogeneity on high resolution ionexchange chromatography.EMBO J 2: 2065–2069, 1983.

    Google Scholar 

  199. Butterworth, P., Barlow, J., Konialis, C., Povey, S., and Edwards, Y.H.: The assignment of human erythrocyte carbonic anhydrase CA1 to chromosome 8.Cytogenet Cell Genet 40: 597, 1985.

    Google Scholar 

  200. Caccia, N., Kronenberg, M., Saxe, D., Haars, R., Bruns, G.A.P., Goverman, J., Malissen, M., Willard, H., Yoshikai, Y., Simon, M., and Hood, L.: The T cell receptor beta-chain genes are located on chromosome 6 in mice and chromosome 7 in humans.Cell 37: 1091–1099, 1984.

    Google Scholar 

  201. Cahilly, L.A. and George, D.L.: Regional mapping ofcKi-ras proto-oncogene on mouse chromosome 6 by in situ hybridization.Cytogenet Cell Genet 39: 140–144, 1985.

    Google Scholar 

  202. Cahilly, L.A., George, D., Daugherty, B.L., and Petska, S.: Subchromosomal localization of mouseIFN-alpha genes by in situ hybridization.J Interferon Res 5: 391–395, 1985.

    Google Scholar 

  203. Calabi, F. and Milstein, C.: A novel family of human major histocompatibility complex-related genes not mapping to chromosome 6.Nature 323: 540–543, 1986.

    Google Scholar 

  204. Callen, D.F., Baker, E., Hyland, V., Frantini, A., Simmers, R., Mulley, J.C., and Sutherland, G.R.: Physical mapping of band 16q22 by in situ hybridization.Cytogenet Cell Genet 46: 589, 1987.

    Google Scholar 

  205. Camerino, G., Grzeschik, K.H., Jaye, M., De La Salle, H., Tolstoshev, P., Lecocq, J.P., Heilig, R., and Mandel, J.L.: Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus).Proc Natl Acad Sci USA 81: 498–502, 1984.

    Google Scholar 

  206. Campbell, K., Flavin, N., Ivens, A., Robert, B., Buckingham, M., and Williamson, R.: The human homeobox geneHOX7 maps to 4p16.1 and is deleted in Wolf-Hirschhorn syndrome patients.Am J Hum Genet 45: A178, 1989.

    Google Scholar 

  207. Campbell, G.R., Zimmerman, K., Blank, R.D., Alt, F.W., and D'Eustachio, P.: Chromosomal location of N-myc and L-myc genes in the mouse.Oncogene Res 4: 47–54, 1989.

    Google Scholar 

  208. Cannizzaro, L.A., Bollum, F.J., Huebner, J., Croce, C.M., Cheung, L.C., Xu, X., Hecht, B.K., and Chang, L.M.S.: Chromosome sublocation of a cDNA for human DNA polymerase-beta to 8p11-p12.Cytogenet Cell Genet 47: 121–124, 1988.

    Google Scholar 

  209. Cannizzaro, L.A., Bollum, F.J., Huebner, K., Croce, C.M., Cheung, L.C., Xuq, X., Hecht, B.K., Hecht, F. and Chang, L.M.S.: Molecular cloning and chromosome sublocation of a cDNA for human DNA polymerase to 8p11-8p12.Cytogenet Cell Genet 46: 589, 1987.

    Google Scholar 

  210. Cannizzaro, L.A., Croce, C.M., Griffen, C.A., Simone, A., Boncineli, E., and Huebner, K.: Human homeobox-containing genes located at chromosome regions 2q31-2q37 and 12q12-12q13.Am J Hum Genet 41: 1–15, 1987.

    Google Scholar 

  211. Cannizzaro, L.A., Emanuel, B.S., Cho, K.W.Y., and Weinmann, R.: The gene encoding the large subunit of human RNA polymerase II is located on the short arm of human chromosome 17.Am J Hum Genet 38: 812–818, 1986.

    Google Scholar 

  212. Carlock, L., Hiroshige, S., Wasmuth, J., and Smith, M.: Assignment of theADH5 gene coding for class III ADH to human chromosome 4: 4q21-4q25.Cytogenet Cell Genet 40: 598, 1985.

    Google Scholar 

  213. Carlson, G.A., Goodman, P.A., Lovett, M., Taylor, B.A., Marshall, S.T., Peterson-Torchia, M., Westaway, D., and Prusiner, S.B.: Genetics and polymorphism of the mouse prion gene complex: control of scrapie incubation time.Mol Cell Biol 8: 5528–5540, 1988.

    Google Scholar 

  214. Carlson, M., Nakamura, Y., Gillilan, S., O'Connell, P.O., Lebo, R., Gorin, F., Lathrop, G.M., Lalouel, J.M., and White, R.: Isolation and mapping of a polymorphic DNA sequence for human glycogen phosphorylase (pMCMP1) on chromosome 11 (PYGM).Nucleic Acids Res 16: 10403, 1988.

    Google Scholar 

  215. Carritt, B.: Genomic cloning of the short arm of human chromosome 1.Cytogenet Cell Genet 40: 599, 1985.

    Google Scholar 

  216. Carritt, B., Goldfarb, P.S.G., Hooper, M.L., and Slack, C.: Chromosome assignment of a human gene for argininosuccinate synthetase expression in Chinese hamster x human somatic cell hybrids.Exp Cell Res 106: 71–78, 1977.

    Google Scholar 

  217. Carritt, B., King, J., and Welch, H.M.: Gene order and localization of enzyme loci on the short arm of chromosome 1.Ann Hum Genet 46: 329–335, 1982.

    Google Scholar 

  218. Carroll, M.C., Campbell, R.D., Bentley, D.R., and Porter, R.R.: A molecular map of the human histocompatibility complex class III region linking complement genesC4, C2 andfactor B.Nature 307: 237–241, 1984.

    Google Scholar 

  219. Carroll, M.C., Katzman, P., Alicot, E.M., Koller, B.H., Geraghty, D.E., Orr, H.T., Strominger, J.L., and Spies, T.: Linkage map of the human major histocompatibility complex including the tumor necrosis factor genes.Proc Natl Acad Sci USA 84: 8535–8539, 1987.

    Google Scholar 

  220. Casey, G., Smith, R., McGillivray, D., Peters, G., and Dickson, C.: Characterization and chromosome assignment of the human homolog ofint-2, a potential proto-oncogene.Mol Cell Biol 6: 502–510, 1986.

    Google Scholar 

  221. Cattanach, B.M.: Location of theXce usingXce〈a〉/Xce〈c〉 heterozygotes.Mouse News Lett 69:24, 1983.

    Google Scholar 

  222. Cattanach, B.M., A new X-linked mutation.Mouse News Lett 66:61–62, 1973.

    Google Scholar 

  223. Caubet, J.F., Mathieu-Mahul, D., Bernheim, A., Larsen, C.J., and Berger, R.: Human proto-oncogene c-mos (MOS) maps to 8q11Cytogenet Cell Genet 40: 602, 1985.

    Google Scholar 

  224. Cavanna, J.S., Coulton, G., Morgan, J.E., Brockdoff, N., Forrest, S.M., Davies, K.E., and Brown, D.M.: Molecular and genetic mapping of the mousemdx locus.Genomics 3: 337–341, 1988.

    Google Scholar 

  225. Cavanna, J.S., Greenfield A.J., Johnson, K.J., Marks, A.R., Nadal-Ginard, B., and Brown, S.D.M.: Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.Genomics 7: 12–18, 1990.

    Google Scholar 

  226. Ceci, J.D., Justice, M.J., Lock, L.F., Jenkins, N.A., and Copeland, N.G.: An interspecific backcross linkage map of mouse chromosome 8.Genomics 6: 72–79, 1990.

    Google Scholar 

  227. Ceci, J.D., Kingsley, D.M., Silan, C.M., Copeland, N.G., and Jenkins, N.A.: An interspecific backeross linkage map of the proximal half of mouse chromosome 14.Genomics 6: 673–678, 1991.

    Google Scholar 

  228. Ceci, J.D., Kingsley, D.M., Silan, C.M., Copeland, N.G., and Jenkins, N.A.: An interspecific backcross linkage map of the proximal half of mouse chromosome 14.Genomics 6: 673–678, 1991.

    Google Scholar 

  229. Ceci J.D., Siracusa, L.D., Jenkins, N.A., and Copeland, N.G.: A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes.Genomics 5: 699–709, 1989.

    Google Scholar 

  230. Chabot, B., Stephenson, D.A., Chapman, V.M., Besmer, P., and Bernstein, A.: The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouseW locus.Nature 335: 88–89, 1988.

    Google Scholar 

  231. Chadefaux, B., Allard, D., Rethore, M.O., Raoul, O., Poissonier, M., Gilgenkrantz, S., Cheruy, C., and Jerome, H.: Assignment of human phosphosribosylglycinamide synthetase locus to region 21q221.Hum Genet 66: 190–192, 1984.

    Google Scholar 

  232. Chaganti, R.S.K., Jhanwar, S.C., Antonarakis, S.E., and Hayward, W.S.: Germ-line chromosomal localization of genes in chromosome lip linkage: parathyroid hormone, betaglobin, c-Ha-ras-1, and insulin.Somatic Cell Mol Genet 11: 197–202, 1985.

    Google Scholar 

  233. Chan, A.M.L., Hilkens, J., Kroezen, V., Mitchell, P.J., Scambler, P., Wainwright, B.J., Williamson, R., and Cooper, C.S.: Molcular cloning and localization to chromosome 6 of mouseINT1L1 gene.Somatic Cell Mol Genet 15: 555–562, 1989.

    Google Scholar 

  234. Chan, T.S., Reardon, M.P., and Greenstein, R.M.: Somatic cell hybrid assignment of a structural gene for human betaglucuronidase to chromosome 7 by use of an X/7 translocation.Cytogenet Cell Genet 17: 291–295, 1976.

    Google Scholar 

  235. Chance, P.F., Dyer, K.A., Kurachi, K., Yoshitake, S., Ropers, H.O., Wieacker, P., and Gartler, S.M.: Regional assignment of the human factor IX gene by molecular hybridization.Cytogenet Cell Genet 37: 435, 1984.

    Google Scholar 

  236. Chandrasekharappa, S.C., Rebelsky, M.S., Firak, T.A., Le Beau, M.M., and Westbrook, C.A.: A long-range restriction map of the interleukin-4 and interleukin-5 linkage group on chromosome 5.Genomics 6: 94–99, 1990.

    Google Scholar 

  237. Chang, K.S., Schroeder, W., Sicilano, M.J., Thompson, L.H., McCredie, K., Beran, M., Freireich, E.J., Liang, J.C., Trujillo, J.M., and Stass, S.A.: The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia.Leukemia 1:458–462, 1987.

    Google Scholar 

  238. Chany, C., Vignal, M., Couillin, P., Nguyen, V.C., Boue, J., and Boue, A.: Chromosomal localization of human gene governing the interferon-induced antiviral state.Proc Natl Acad Sci USA 72: 3129–3133, 1975.

    Google Scholar 

  239. Chapman, V.M.,[Bgl-s]. Mouse News Lett 49: 46, 1973.

    Google Scholar 

  240. Chapman, V.M. and Frels, W.: [Map order on Chromosome 9].Mouse News Lett 53: 61, 1975.

    Google Scholar 

  241. Chapman, V.M., Keitz, B.T., Stephenson, D.A., Mullins, L.J., Moos, M., and Shachner, M.: Linkage of a gene for neural cell adhesion molecule, L1 (CamL1) to the Rsvp region of the mouse X chromosome.Genomics 5: 113–118, 1990.

    Google Scholar 

  242. Chapman, V.M., Keitz, B.T., Disteche, C.M., Lau, E.C., and Snead, M.L.: Linkage of amelogenin (Amel) to the distal portion of the mouse X chromosome.Genomics 10: 23–28, 1991.

    Google Scholar 

  243. Chapman, V.M., Kratzer, P.G., and Quarantillo, B.A.: Electrophoretic variation for X chromosome-linked hypoxanthine phosphoribosyl transferase (HPRT) in wild-derived mice.Genetics 103: 785–795, 1983.

    Google Scholar 

  244. Chapman, V.M., Mullins, L.J., Grant, S.G., and Stephenson, D.A.: X-chromosome gene mapping using twoMus species hybrids.Mouse News Lett 79: 64, 1987.

    Google Scholar 

  245. Chapman, V.M., Murawski, M., Miller, D., and Swiatek, D.: Linkage analyses of X-chromosome-linked muscular dystrophy,mdx.Mouse News Lett 72: 120, 1985.

    Google Scholar 

  246. Chapman, V.M. and Ruddle, F.H.: Glutamate oxaloacetate transaminase (GOT) genetics in the mouse: polymorphism ofGot-1.Genetics 70: 299–305, 1972.

    Google Scholar 

  247. Chapman, V.M., Ruddle, F.H., and Roderick, T.H.: Linkage of isozyme loci in the mouse: phosphoglucomutase-2 (Pgm-2), mitochondrial NADP malate dehydrogenase (Mod-2) and dipeptidase-1 (Dip-1).Biochem Genet 5: 101–110, 1971.

    Google Scholar 

  248. Chapman, V.M. and Shows, T.B.: Somatic cell genetic evidence for X-chromosome linkage of three enzymes in the mouse.Nature 259: 665–667, 1976.

    Google Scholar 

  249. Chapman, V.M., Stephenson, D.A., Mullins, L.J., Keitz, B.T., Disteche, C., and Orkin, S.H.: Linkage of the erythroid transcription factor gene (Gf-1) to the proximal region of the X chromosome of mice.Genomics 9: 309–311, 1991.

    Google Scholar 

  250. Charmley, P., Nguyen, J., Wei, S., and Gatti, R.A.: Genetic analysis and homology relationships of genes located on human chromosome 11q.Genomics 10:608–617, 1991.

    Google Scholar 

  251. Chavrier, P., Janssen-Timmen, U., Mattei, M.G., Zerial, M., Bravo, R., and Charnay, P.: Structure, chromosome location, and expression of the mouse zinc finger geneKrox-20: multiple gene products and coregulation with the proto-oncogene c-fos.Mol Cell Biol 9: 787–797, 1989.

    Google Scholar 

  252. Cheah, K.S.E., Au, P.K.C., Lau, E.T., Little, P.F.R., and Stubbs, L.: The mouseCol2a-1 gene is highly conserved and is linked toInt-1 on chromosome 15.Mammalian Genome 1: 171–183, 1991.