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Journal Abstract Search


320 related items for PubMed ID: 3473444

  • 1. Physical and genetic analysis of cosmids from the vicinity of the cystic fibrosis locus.
    Scambler PJ, Estivill X, Bell G, Farrall M, McLean C, Newman R, Little PF, Frederick P, Hawley K, Wainwright BJ.
    Nucleic Acids Res; 1987 May 11; 15(9):3639-52. PubMed ID: 3473444
    [Abstract] [Full Text] [Related]

  • 2. Isolation of a new DNA marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP.
    Estivill X, McLean C, Nunes V, Casals T, Gallano P, Scambler P, Williamson R.
    Am J Hum Genet; 1989 May 11; 44(5):704-10. PubMed ID: 2565082
    [Abstract] [Full Text] [Related]

  • 3. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q.
    Buroker NE, Magenis RE, Weliky K, Bruns G, Litt M.
    Hum Genet; 1986 Jan 11; 72(1):86-94. PubMed ID: 3002956
    [Abstract] [Full Text] [Related]

  • 4. Physical mapping of complex genomes by cosmid multiplex analysis.
    Evans GA, Lewis KA.
    Proc Natl Acad Sci U S A; 1989 Jul 11; 86(13):5030-4. PubMed ID: 2740339
    [Abstract] [Full Text] [Related]

  • 5. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
    Rouquier S, Giorgi D, Trask B, Bergmann A, Phillips MS, MacLennan DH, de Jong P.
    Genomics; 1993 Aug 11; 17(2):330-40. PubMed ID: 8406483
    [Abstract] [Full Text] [Related]

  • 6. A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library.
    Bufton L, Mohandas TK, Magenis RE, Sheehy R, Bestwick RK, Litt M.
    Hum Genet; 1986 Dec 11; 74(4):425-31. PubMed ID: 2878870
    [Abstract] [Full Text] [Related]

  • 7. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
    Hofker MH, Bergen AA, Skraastad MI, Carpenter NJ, Veenema H, Connor JM, Bakker E, van Ommen GJ, Pearson PL.
    Am J Hum Genet; 1987 Apr 11; 40(4):312-28. PubMed ID: 2883888
    [Abstract] [Full Text] [Related]

  • 8. Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndrome.
    Kurahashi H, Akagi K, Karakawa K, Nakamura T, Dumanski JP, Sano T, Okada S, Takai S, Nishisho I.
    Hum Genet; 1994 Mar 11; 93(3):248-54. PubMed ID: 7907312
    [Abstract] [Full Text] [Related]

  • 9. Studies on locus expansion, library representation, and chromosome walking using an efficient method to screen cosmid libraries.
    Bowden DW, Müller-Kahle H, Fulton TR, Gravius TC, Barker DF, Donis-Keller H.
    Gene; 1988 Nov 30; 71(2):391-400. PubMed ID: 2906313
    [Abstract] [Full Text] [Related]

  • 10. Localization of 616 human chromosome 3-specific cosmids using a somatic cell hybrid deletion mapping panel.
    Smith DI, Liu W, Ginzinger D, Green P, Smith S, Wang ND, Recchia F, Carolyn K, Drabkin H, Golembieski W.
    Genomics; 1991 Sep 30; 11(1):179-87. PubMed ID: 1662664
    [Abstract] [Full Text] [Related]

  • 11. 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 30; 17(3):682-93. PubMed ID: 8244385
    [Abstract] [Full Text] [Related]

  • 12. Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene.
    Rommens JM, Zengerling S, Burns J, Melmer G, Kerem BS, Plavsic N, Zsiga M, Kennedy D, Markiewicz D, Rozmahel R.
    Am J Hum Genet; 1988 Nov 30; 43(5):645-63. PubMed ID: 2903665
    [Abstract] [Full Text] [Related]

  • 13. Development of 124 sequence-tagged sites and cytogenetic localization of 217 cosmids for human chromosome 10.
    Zheng CJ, Ma NS, Dorman TE, Wang MT, Braunschweiger K, Soares L, Schuster MK, Rothschild CB, Bowden DW, Torrey D.
    Genomics; 1994 Jul 01; 22(1):55-67. PubMed ID: 7959792
    [Abstract] [Full Text] [Related]

  • 14. A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis.
    Ramsay M, Wainwright BJ, Farrall M, Estivill X, Sutherland H, Ho MF, Davies R, Halford S, Tata F, Wicking C.
    Genomics; 1990 Jan 01; 6(1):39-47. PubMed ID: 1968045
    [Abstract] [Full Text] [Related]

  • 15. Progress towards construction of a total restriction fragment map of a human chromosome.
    Vissing H, Grosveld F, Solomon E, Moore G, Lench N, Shennan N, Williamson R.
    Nucleic Acids Res; 1987 Feb 25; 15(4):1363-75. PubMed ID: 3029713
    [Abstract] [Full Text] [Related]

  • 16. A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.
    Litt M, Bruns GA, Sheehy R, Magenis RE.
    Am J Hum Genet; 1986 Mar 25; 38(3):288-96. PubMed ID: 3006480
    [Abstract] [Full Text] [Related]

  • 17. Isolation of a polymorphic genomic clone from chromosome 7. Physical and genetic linkage studies to markers around the cystic fibrosis locus.
    Davies KA, Lorand L, Waterfield M, Wainwright B, Farrall M, Williamson R.
    Hum Genet; 1987 Oct 25; 77(2):122-6. PubMed ID: 2888718
    [Abstract] [Full Text] [Related]

  • 18. Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions.
    Hou DX, Kishida H, Shimokawa T, Soeda E.
    Jpn J Hum Genet; 1994 Dec 25; 39(4):411-20. PubMed ID: 7873753
    [Abstract] [Full Text] [Related]

  • 19. A highly polymorphic locus in human DNA revealed by cosmid-derived probes.
    Litt M, White RL.
    Proc Natl Acad Sci U S A; 1985 Sep 25; 82(18):6206-10. PubMed ID: 2994065
    [Abstract] [Full Text] [Related]

  • 20. Isolation of two contigs of overlapping cosmids derived from human chromosomal band 3p21.1 and identification of 5 new 3p21.1 genes.
    Shridhar V, Golembieski W, Kamat A, Smith SE, Phillips N, Miller OJ, Miller Y, Smith DI.
    Somat Cell Mol Genet; 1994 Jul 25; 20(4):255-65. PubMed ID: 7974002
    [Abstract] [Full Text] [Related]


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