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Journal Abstract Search

210 related items for PubMed ID: 8808277

  • 1. Refined mapping and YAC contig construction of the X-linked cleft palate and ankyloglossia locus (CPX) including the proximal X-Y homology breakpoint within Xq21.3.
    Forbes SA, Brennan L, Richardson M, Coffey A, Cole CG, Gregory SG, Bentley DR, Mumm S, Moore GE, Stanier P.
    Genomics; 1996 Jan 01; 31(1):36-43. PubMed ID: 8808277
    [Abstract] [Full Text] [Related]

  • 2. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X.
    Stanier P, Forbes SA, Arnason A, Bjornsson A, Sveinbjornsdottir E, Williamson R, Moore G.
    Genomics; 1993 Sep 01; 17(3):549-55. PubMed ID: 8244369
    [Abstract] [Full Text] [Related]

  • 3. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
    Mitsuda N, Nakura J, Ye L, Zhao Y, Fujioka Y, Takahashi-Fujii A, Ishino Y, Kato I, Hashimoto K, Ogihara T, Miki T.
    Genomics; 1997 Apr 01; 41(1):49-55. PubMed ID: 9126481
    [Abstract] [Full Text] [Related]

  • 4. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
    Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, Seemayer TA, Klein G, Purtilo DT, Sumegi J.
    Genomics; 1997 Jan 01; 39(1):55-65. PubMed ID: 9027486
    [Abstract] [Full Text] [Related]

  • 5. Refinement of the Van der Woude gene location and construction of a 3.5-Mb YAC contig and STS map spanning the critical region in 1q32-q41.
    Schutte BC, Sander A, Malik M, Murray JC.
    Genomics; 1996 Sep 15; 36(3):507-14. PubMed ID: 8884274
    [Abstract] [Full Text] [Related]

  • 6. Refinement of the X-linked cleft palate and ankyloglossia (CPX) localisation by genetic mapping in an Icelandic kindred.
    Forbes SA, Richardson M, Brennan L, Arnason A, Bjornsson A, Campbell L, Moore G, Stanier P.
    Hum Genet; 1995 Mar 15; 95(3):342-6. PubMed ID: 7868130
    [Abstract] [Full Text] [Related]

  • 7. Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region.
    Braybrook C, Warry G, Howell G, Mandryko V, Arnason A, Bjornsson A, Ross MT, Moore GE, Stanier P.
    Hum Genet; 2001 Jun 15; 108(6):537-45. PubMed ID: 11499681
    [Abstract] [Full Text] [Related]

  • 8. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA, Roth EJ, McCabe ER, Chinault AC, Zoghbi HY.
    Am J Med Genet; 1993 Nov 15; 47(7):1124-34. PubMed ID: 8291533
    [Abstract] [Full Text] [Related]

  • 9. Integrated STS/YAC physical, genetic, and transcript map of human Xq21.3 to q23/q24 (DXS1203-DXS1059).
    Srivastava AK, McMillan S, Jermak C, Shomaker M, Copeland-Yates SA, Sossey-Alaoui K, Mumm S, Schlessinger D, Nagaraja R.
    Genomics; 1999 Jun 01; 58(2):188-201. PubMed ID: 10366451
    [Abstract] [Full Text] [Related]

  • 10. Yeast artificial chromosome cloning of 3.2 megabases within chromosomal band 11q24 closely linking c-ets 1 and Fli-1 and encompassing the Ewing sarcoma breakpoint.
    Selleri L, Giovannini M, Hermanson GG, Romo A, Quackenbush J, Penny L, Khristich JV, Evans GA.
    Genomics; 1994 Jul 01; 22(1):137-47. PubMed ID: 7959760
    [Abstract] [Full Text] [Related]

  • 11. A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.
    Lee WC, Ferrero GB, Chinault AC, Yen PH, Ballabio A.
    Genomics; 1993 Oct 01; 18(1):1-6. PubMed ID: 8276392
    [Abstract] [Full Text] [Related]

  • 12. Localization of a mutant gene for cleft palate and ankyloglossia in an X-linked Icelandic family.
    Moore GE, Williamson R, Jensson O, Chambers J, Takakubo F, Newton R, Balacs MA, Ivens A.
    J Craniofac Genet Dev Biol; 1991 Oct 01; 11(4):372-6. PubMed ID: 1687471
    [Abstract] [Full Text] [Related]

  • 13. The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.
    Sumegi J, Wang JY, Zhen DK, Eudy JD, Talmadge CB, Li BF, Berglund P, Weston MD, Yao SF, Ma-Edmonds M, Overbeck L, Kelley PM, Zabarovsky E, Uzvolgyi E, Stanbridge EJ, Klein G, Kimberling WJ.
    Genomics; 1996 Jul 01; 35(1):79-86. PubMed ID: 8661107
    [Abstract] [Full Text] [Related]

  • 14. Identification and characterization of KLHL4, a novel human homologue of the Drosophila Kelch gene that maps within the X-linked cleft palate and Ankyloglossia (CPX) critical region.
    Braybrook C, Warry G, Howell G, Arnason A, Bjornsson A, Moore GE, Ross MT, Stanier P.
    Genomics; 2001 Mar 01; 72(2):128-36. PubMed ID: 11401425
    [Abstract] [Full Text] [Related]

  • 15. A complete YAC contig and cosmid interval map covering the entirety of human Xq21.33 to Xq22.3 from DXS3 to DXS287.
    Kendall E, Evans W, Jin H, Holland J, Vetrie D.
    Genomics; 1997 Jul 15; 43(2):171-82. PubMed ID: 9244434
    [Abstract] [Full Text] [Related]

  • 16. A 4.5-megabase YAC contig and physical map over the hemochromatosis gene region.
    Burt MJ, Smit DJ, Pyper WR, Powell LW, Jazwinska EC.
    Genomics; 1996 Apr 15; 33(2):153-8. PubMed ID: 8660962
    [Abstract] [Full Text] [Related]

  • 17. Sequence-ready BAC contig, physical, and transcriptional map of a 2-Mb region overlapping the mouse chromosome 6 host-resistance locus Cmv1.
    Depatie C, Lee SH, Stafford A, Avner P, Belouchi A, Gros P, Vidal SM.
    Genomics; 2000 Jun 01; 66(2):161-74. PubMed ID: 10860661
    [Abstract] [Full Text] [Related]

  • 18. A 2-Mb YAC contig and physical map covering the chromosome 8q12 breakpoint cluster region in pleomorphic adenomas of the salivary glands.
    Kas K, Röijer E, Voz M, Meyen E, Stenman G, Van de Ven WJ.
    Genomics; 1997 Aug 01; 43(3):349-58. PubMed ID: 9268638
    [Abstract] [Full Text] [Related]

  • 19. High-resolution physical mapping of a 6.7-Mb YAC contig spanning a region critical for the monosomy 21 phenotype in 21q21.3-q22.1.
    Orti R, Mégarbane A, Maunoury C, Van Broeckhoven C, Sinet PM, Delabar JM.
    Genomics; 1997 Jul 01; 43(1):25-33. PubMed ID: 9226369
    [Abstract] [Full Text] [Related]

  • 20. [Yeast artificial chromosome cloning and physical mapping of retinitis pigmentosa 3 (RP3) locus].
    Miao W, Wei Y, Deng W.
    Zhonghua Yi Xue Za Zhi; 1996 Oct 01; 76(10):747-9. PubMed ID: 9275515
    [Abstract] [Full Text] [Related]

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