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Journal Abstract Search

220 related items for PubMed ID: 7587392

  • 41. A 4-megabase YAC contig that spans the Langer-Giedion syndrome region on human chromosome 8q24.1: use in refining the location of the trichorhinophalangeal syndrome and multiple exostoses genes (TRPS1 and EXT1).
    Hou J, Parrish J, Lüdecke HJ, Sapru M, Wang Y, Chen W, Hill A, Siegel-Bartelt J, Northrup H, Elder FF.
    Genomics; 1995 Sep 01; 29(1):87-97. PubMed ID: 8530105
    [Abstract] [Full Text] [Related]

  • 42. Characterization of a voltage-activated K-channel gene cluster on human chromosome 12p13.
    Albrecht B, Weber K, Pongs O.
    Recept Channels; 1995 Sep 01; 3(3):213-20. PubMed ID: 8821794
    [Abstract] [Full Text] [Related]

  • 43. Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpoint.
    de Leeuw B, Balemans M, Weghuis DO, Seruca R, Janz M, Geraghty MT, Gilgenkrantz S, Ropers HH, Geurts van Kessel A.
    Hum Mol Genet; 1994 May 01; 3(5):745-9. PubMed ID: 8081361
    [Abstract] [Full Text] [Related]

  • 44. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
    Paradee W, Wilke CM, Wang L, Shridhar R, Mullins CM, Hoge A, Glover TW, Smith DI.
    Genomics; 1996 Jul 01; 35(1):87-93. PubMed ID: 8661108
    [Abstract] [Full Text] [Related]

  • 45. Construction of a 3.7-Mb physical map within human chromosome 20p12 ordering 18 markers in the Alagille syndrome locus.
    Pollet N, Dhorne-Pollet S, Deleuze JF, Boccaccio C, Driancourt C, Raynaud N, Le Paslier D, Hadchouel M, Meunier-Rotival M.
    Genomics; 1995 Jun 10; 27(3):467-74. PubMed ID: 7558028
    [Abstract] [Full Text] [Related]

  • 46. Fish mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia.
    Kato R, Matsumoto N, Fujimoto M, Nakano M, Nakamura Y, Niikawa N.
    Jpn J Hum Genet; 1997 Dec 10; 42(4):525-32. PubMed ID: 9560952
    [Abstract] [Full Text] [Related]

  • 47. Cloning and characterization of the human t(3;6)(p14;p11) translocation breakpoint associated with hematologic malignancies.
    Smith SE, Joseph A, Nadeau S, Shridhar V, Gemmill R, Drabkin H, Knuutila S, Smith DI.
    Cancer Genet Cytogenet; 1993 Nov 10; 71(1):15-21. PubMed ID: 8275448
    [Abstract] [Full Text] [Related]

  • 48. Identification of a yeast artificial chromosome spanning the 8q12 translocation breakpoint in pleomorphic adenomas with t(3;8)(p21;q12).
    Röijer E, Kas K, Klawitz I, Bullerdiek J, Van de Ven W, Stenman G.
    Genes Chromosomes Cancer; 1996 Nov 10; 17(3):166-71. PubMed ID: 8946195
    [Abstract] [Full Text] [Related]

  • 49. Microdissection based cloning of a translocation breakpoint in a human malignant melanoma.
    Zhang J, Cui P, Glatfelter AA, Cummings LM, Meltzer PS, Trent JM.
    Cancer Res; 1995 Oct 15; 55(20):4640-5. PubMed ID: 7553642
    [Abstract] [Full Text] [Related]

  • 50. Integrated physical, genetic, and genic map covering 3 Mb around the human NGF gene (NGFB) at 1p13.
    Carrier A, Rosier MF, Guillemot F, Goguel AF, Pulcini F, Bernheim A, Auffray C, Devignes MD.
    Genomics; 1996 Jan 01; 31(1):80-9. PubMed ID: 8808283
    [Abstract] [Full Text] [Related]

  • 51. FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6.
    Bray-Ward P, Bowlus C, Choi J, Paslier DL, Weissenbach J, Gruen JR.
    Genomics; 1996 Aug 15; 36(1):104-11. PubMed ID: 8812421
    [Abstract] [Full Text] [Related]

  • 52. Isolation of a 370 kb YAC fragment spanning a translocation breakpoint at 3p14.1 associated with holoprosencephaly.
    Petek E, Kroisel PM, Wagner K.
    Clin Genet; 1998 Nov 15; 54(5):406-12. PubMed ID: 9842993
    [Abstract] [Full Text] [Related]

  • 53. A 1.8-Mb YAC contig in Xp11.23: identification of CpG islands and physical mapping of CA repeats in a region of high gene density.
    Coleman MP, Németh AH, Campbell L, Raut CP, Weissenbach J, Davies KE.
    Genomics; 1994 May 15; 21(2):337-43. PubMed ID: 8088827
    [Abstract] [Full Text] [Related]

  • 54. The generation and regional localization of 303 new chromosome 5 sequence-tagged sites.
    Grady DL, Robinson DL, Gersh M, Nickerson E, McPherson J, Wasmuth JJ, Overhauser J, Deaven LL, Moyzis RK.
    Genomics; 1996 Feb 15; 32(1):91-6. PubMed ID: 8786125
    [Abstract] [Full Text] [Related]

  • 55. Isolation of yeast artificial chromosomes containing the entire transcriptional unit of the human FGF1 gene: a 720-kb contig spanning human chromosome 5q31.3-->q32.
    Chiu IM, Liu Y, Payson RA.
    Cancer Genet Cytogenet; 1998 Oct 01; 106(1):1-10. PubMed ID: 9772902
    [Abstract] [Full Text] [Related]

  • 56. Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation.
    Matsumoto N, Pilz DT, Fantes JA, Kittikamron K, Ledbetter DH.
    J Med Genet; 1998 Oct 01; 35(10):829-32. PubMed ID: 9783706
    [Abstract] [Full Text] [Related]

  • 57. Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
    Schoenmakers EF, Kools PF, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong PJ, Van den Berghe H, Van de Ven WJ.
    Genomics; 1994 Mar 15; 20(2):210-22. PubMed ID: 8020967
    [Abstract] [Full Text] [Related]

  • 58. Characterization and chromosomal assignment of yeast artificial chromosomes containing human 3p13-p21-specific sequence tagged sites.
    Michaelis SC, Bardenheuer W, Lux A, Schramm A, Gockel A, Siebert R, Willers C, Schmidtke K, Todt B, van der Hout AH.
    Cancer Genet Cytogenet; 1995 May 15; 81(1):1-12. PubMed ID: 7773951
    [Abstract] [Full Text] [Related]

  • 59. An integrated physical and genetic map spanning chromosome band 10q24.
    Gray IC, Fallowfield J, Ford S, Nobile C, Volpi EV, Spurr NK.
    Genomics; 1997 Jul 01; 43(1):85-8. PubMed ID: 9226376
    [Abstract] [Full Text] [Related]

  • 60. Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.
    Banfi S, Chung MY, Kwiatkowski TJ, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY.
    Genomics; 1993 Dec 01; 18(3):627-35. PubMed ID: 8307572
    [Abstract] [Full Text] [Related]

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