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484 related items for PubMed ID: 9177769

  • 1. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
    Wilgenbus KK, Seranski P, Brown A, Leuchs B, Mincheva A, Lichter P, Poustka A.
    Genomics; 1997 May 15; 42(1):1-10. PubMed ID: 9177769
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
    Seranski P, Heiss NS, Dhorne-Pollet S, Radelof U, Korn B, Hennig S, Backes E, Schmidt S, Wiemann S, Schwarz CE, Lehrach H, Poustka A.
    Genomics; 1999 Feb 15; 56(1):1-11. PubMed ID: 10036180
    [Abstract] [Full Text] [Related]

  • 4. An integrated high-resolution physical map of the DPC/BRCA2 region at chromosome 13q12.
    Schutte M, Rozenblum E, Moskaluk CA, Guan X, Hoque AT, Hahn SA, da Costa LT, de Jong PJ, Kern SE.
    Cancer Res; 1995 Oct 15; 55(20):4570-4. PubMed ID: 7553631
    [Abstract] [Full Text] [Related]

  • 5. Molecular cloning of the interleukin-1 gene cluster: construction of an integrated YAC/PAC contig and a partial transcriptional map in the region of chromosome 2q13.
    Nothwang HG, Strahm B, Denich D, Kübler M, Schwabe J, Gingrich JC, Jauch A, Cox A, Nicklin MJ, Kurnit DM, Hildebrandt F.
    Genomics; 1997 May 01; 41(3):370-8. PubMed ID: 9169134
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. 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]

  • 9. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
    Francis F, Benham F, See CG, Fox M, Ishikawa-Brush Y, Monaco AP, Weiss B, Rappold G, Hamvas RM, Lehrach H.
    Genomics; 1994 Mar 01; 20(1):75-83. PubMed ID: 8020959
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Construction of a 5-Mb YAC contig from the putative 10q25 tumor-suppressor region for glioblastomas.
    Albarosa R, Finocchiaro G, Chiariello E, Russo G, Susani L, Vezzoni P, Zucchi I.
    Genomics; 1997 May 01; 41(3):345-9. PubMed ID: 9169131
    [Abstract] [Full Text] [Related]

  • 12. YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.
    Wedemeyer N, Lengeling A, Ronsiek M, Korthaus D, Baer K, Wuttke M, Jockusch H.
    Genomics; 1996 Mar 15; 32(3):447-54. PubMed ID: 8838809
    [Abstract] [Full Text] [Related]

  • 13. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
    Yu CE, Oshima J, Hisama FM, Matthews S, Trask BJ, Schellenberg GD.
    Genomics; 1996 Aug 01; 35(3):431-40. PubMed ID: 8812476
    [Abstract] [Full Text] [Related]

  • 14. Closing in on the BPES gene on 3q23: mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and beta'-COP, distal to the breakpoint.
    De Baere E, Van Roy N, Speleman F, Fukushima Y, De Paepe A, Messiaen L.
    Genomics; 1999 Apr 01; 57(1):70-8. PubMed ID: 10191085
    [Abstract] [Full Text] [Related]

  • 15. Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysis.
    Lucas RE, Vlangos CN, Das P, Patel PI, Elsea SH.
    Eur J Hum Genet; 2001 Dec 01; 9(12):892-902. PubMed ID: 11840190
    [Abstract] [Full Text] [Related]

  • 16. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC, de Luis O, Cruces J, Pérez Jurado LA.
    Genomics; 2000 Oct 01; 69(1):1-13. PubMed ID: 11013070
    [Abstract] [Full Text] [Related]

  • 17. Characterization of two chromosome 12 cosmid libraries and development of STSs from cosmids mapped by FISH.
    Montgomery KT, LeBlanc JM, Tsai P, McNinch JS, Ward DC, de Jong PJ, Kucherlapati R, Krauter KS.
    Genomics; 1993 Sep 01; 17(3):682-93. PubMed ID: 8244385
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. 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]

  • 20. YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.
    Miyake M, Nakahori Y, Matsushita I, Kobayashi K, Mizuno K, Hirai M, Kanazawa I, Nakagome Y, Tokunaga K, Toda T.
    Genomics; 1997 Mar 01; 40(2):284-93. PubMed ID: 9119396
    [Abstract] [Full Text] [Related]

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