These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

148 related items for PubMed ID: 8188260

  • 1. Precise mapping of the brain alpha 2-adrenergic receptor gene within chromosome 4p16.
    Riess O, Thies U, Siedlaczck I, Potisek S, Graham R, Theilmann J, Grimm T, Epplen JT, Hayden MR.
    Genomics; 1994 Jan 15; 19(2):298-302. PubMed ID: 8188260
    [Abstract] [Full Text] [Related]

  • 2. Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3.
    McCombie WR, Martin-Gallardo A, Gocayne JD, FitzGerald M, Dubnick M, Kelley JM, Castilla L, Liu LI, Wallace S, Trapp S.
    Nat Genet; 1992 Aug 15; 1(5):348-53. PubMed ID: 1338771
    [Abstract] [Full Text] [Related]

  • 3. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene.
    Baxendale S, MacDonald ME, Mott R, Francis F, Lin C, Kirby SF, James M, Zehetner G, Hummerich H, Valdes J.
    Nat Genet; 1993 Jun 15; 4(2):181-6. PubMed ID: 8348156
    [Abstract] [Full Text] [Related]

  • 4. Cloning of the human dopamine D5 receptor gene and identification of a highly polymorphic microsatellite for the DRD5 locus that shows tight linkage to the chromosome 4p reference marker RAF1P1.
    Sherrington R, Mankoo B, Attwood J, Kalsi G, Curtis D, Buetow K, Povey S, Gurling H.
    Genomics; 1993 Nov 15; 18(2):423-5. PubMed ID: 8288248
    [Abstract] [Full Text] [Related]

  • 5. Non-random association between DNA markers and Huntington disease locus in the Italian population.
    Novelletto A, Mandich P, Bellone E, Malaspina P, Vivona G, Ajmar F, Frontali M.
    Am J Med Genet; 1991 Sep 01; 40(3):374-6. PubMed ID: 1683157
    [Abstract] [Full Text] [Related]

  • 6. Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease.
    Goldberg YP, Rommens JM, Andrew SE, Hutchinson GB, Lin B, Theilmann J, Graham R, Glaves ML, Starr E, McDonald H.
    Nature; 1993 Mar 25; 362(6418):370-3. PubMed ID: 8384324
    [Abstract] [Full Text] [Related]

  • 7. 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 25; 17(3):682-93. PubMed ID: 8244385
    [Abstract] [Full Text] [Related]

  • 8. Frequency and polymorphism of simple sequence repeats in a contiguous 685-kb DNA sequence containing the human T-cell receptor beta-chain gene complex.
    Charmley P, Concannon P, Hood L, Rowen L.
    Genomics; 1995 Oct 10; 29(3):760-5. PubMed ID: 8575771
    [Abstract] [Full Text] [Related]

  • 9. A novel tandem repeat sequence located on human chromosome 4p: isolation and characterization.
    Kogi M, Fukushige S, Lefevre C, Hadano S, Ikeda JE.
    Genomics; 1997 Jun 01; 42(2):278-83. PubMed ID: 9192848
    [Abstract] [Full Text] [Related]

  • 10. (CA)n-dinucleotide repeat polymorphism at the locus for the alpha2C adrenergic receptor (ADRA2C) on 4p16.
    Riess O, Weber B, Hayden MR.
    Hum Mol Genet; 1992 Sep 01; 1(6):452. PubMed ID: 1338762
    [No Abstract] [Full Text] [Related]

  • 11. Cloning and mapping of the alpha-adducin gene close to D4S95 and assessment of its relationship to Huntington disease.
    Goldberg YP, Lin BY, Andrew SE, Nasir J, Graham R, Glaves ML, Hutchinson G, Theilmann J, Ginzinger DG, Schappert K.
    Hum Mol Genet; 1992 Dec 01; 1(9):669-75. PubMed ID: 1284592
    [Abstract] [Full Text] [Related]

  • 12. Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease.
    Weber B, Riess O, Wolff G, Andrew S, Collins C, Graham R, Theilmann J, Hayden MR.
    Nat Genet; 1992 Nov 01; 2(3):216-22. PubMed ID: 1345172
    [Abstract] [Full Text] [Related]

  • 13. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
    Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH.
    Genomics; 1996 Jun 15; 34(3):299-303. PubMed ID: 8786128
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Mapping of cosmid clones in Huntington's disease region of chromosome 4.
    Whaley WL, Bates GP, Novelletto A, Sedlacek Z, Cheng S, Romano D, Ormondroyd E, Allitto B, Lin C, Youngman S.
    Somat Cell Mol Genet; 1991 Jan 15; 17(1):83-91. PubMed ID: 1671801
    [Abstract] [Full Text] [Related]

  • 18. Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3.
    Andrew S, Theilmann J, Hedrick A, Mah D, Weber B, Hayden MR.
    Genomics; 1992 Jun 15; 13(2):301-11. PubMed ID: 1351866
    [Abstract] [Full Text] [Related]

  • 19. A 370-kb cosmid contig of the serpin gene cluster on human chromosome 14q32.1: molecular linkage of the genes encoding alpha 1-antichymotrypsin, protein C inhibitor, kallistatin, alpha 1-antitrypsin, and corticosteroid-binding globulin.
    Rollini P, Fournier RE.
    Genomics; 1997 Dec 15; 46(3):409-15. PubMed ID: 9441744
    [Abstract] [Full Text] [Related]

  • 20. [Molecular genetics of Huntington's disease].
    Goto J, Masuda N, Watanabe M, Kanazawa I.
    Rinsho Shinkeigaku; 1995 Dec 15; 35(12):1529-31. PubMed ID: 8752453
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.