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Journal Abstract Search

183 related items for PubMed ID: 8244374

  • 1. A high-resolution linkage map of human 9q34.1.
    Henske EP, Ozelius L, Gusella JF, Haines JL, Kwiatkowski DJ.
    Genomics; 1993 Sep; 17(3):587-91. PubMed ID: 8244374
    [Abstract] [Full Text] [Related]

  • 2. A 1.7-megabase sequence-ready cosmid contig covering the TSC1 candidate region in 9q34.
    Hornigold N, van Slegtenhorst M, Nahmias J, Ekong R, Rousseaux S, Hermans C, Halley D, Povey S, Wolfe J.
    Genomics; 1997 May 01; 41(3):385-9. PubMed ID: 9169136
    [Abstract] [Full Text] [Related]

  • 3. A 5.4-Mb continuous pulsed-field gel electrophoresis map of human 9q34.1 between ABL and D9S114, including the tuberous sclerosis (TSC1) region.
    Henske EP, Kwiatkowski DJ.
    Genomics; 1995 Jul 01; 28(1):105-8. PubMed ID: 7590733
    [Abstract] [Full Text] [Related]

  • 4. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
    Todd S, Sherman SL, Naylor SL.
    Genomics; 1993 Jun 01; 16(3):612-8. PubMed ID: 8100800
    [Abstract] [Full Text] [Related]

  • 5. Index, comprehensive microsatellite, and unified linkage maps of human chromosome 14 with cytogenetic tie points and a telomere microsatellite marker.
    Pandit SD, Wang JC, Veile RA, Mishra SK, Warlick CA, Donis-Keller H.
    Genomics; 1995 Oct 10; 29(3):653-64. PubMed ID: 8575758
    [Abstract] [Full Text] [Related]

  • 6. A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference.
    Zahn LM, Kwiatkowski DJ.
    Genomics; 1995 Jul 20; 28(2):140-6. PubMed ID: 8530019
    [Abstract] [Full Text] [Related]

  • 7. Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.
    Harris RM, Carter NP, Griffiths B, Goudie D, Hampson RM, Yates JR, Affara NA, Ferguson-Smith MA.
    Genomics; 1993 Feb 20; 15(2):265-74. PubMed ID: 8449490
    [Abstract] [Full Text] [Related]

  • 8. Absence of linkage of ABO blood group locus to familial tuberous sclerosis.
    Kandt RS, Pericak-Vance MA, Hung WY, Gardner RJ, Nellist M, Phillips K, Warner K, Speer MC, Crossen PE, Laing NG.
    Exp Neurol; 1989 Jun 20; 104(3):223-8. PubMed ID: 2721625
    [Abstract] [Full Text] [Related]

  • 9. Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5.
    Watkins-Chow DE, Buckwalter MS, Newhouse MM, Lossie AC, Brinkmeier ML, Camper SA.
    Genomics; 1997 Feb 15; 40(1):114-22. PubMed ID: 9070927
    [Abstract] [Full Text] [Related]

  • 10. Linkage analysis in two large Italian pedigrees affected with nail patella syndrome.
    Melchionda S, Seri M, Carella M, Piemontese MR, Zhang XX, Zelante L, Romeo G, Gasparini P.
    Eur J Hum Genet; 1998 Feb 15; 6(4):345-9. PubMed ID: 9781042
    [Abstract] [Full Text] [Related]

  • 11. An extended genetic linkage map and an "index" map for human chromosome 17.
    O'Connell P, Plaetke R, Matsunami N, Odelberg S, Jorde L, Chance P, Leppert M, Lalouel JM, White R.
    Genomics; 1993 Jan 15; 15(1):38-47. PubMed ID: 8432550
    [Abstract] [Full Text] [Related]

  • 12. Mapping ESTs to the TSC1 candidate interval by use of the 'Science 96' transcript map.
    Wolfe J, Jeremiah S, Young J, Burley MW, Stewart H, McCulley M, Grant C, Naz K, Povey S.
    Ann Hum Genet; 1997 Sep 15; 61(Pt 5):401-9. PubMed ID: 9459002
    [Abstract] [Full Text] [Related]

  • 13. Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.
    Melis R, Bradley P, Elsner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R.
    Genomics; 1993 Apr 15; 16(1):56-62. PubMed ID: 8486385
    [Abstract] [Full Text] [Related]

  • 14. A linkage map of human chromosome 14, including 13 gene loci.
    Cox DW, Billingsley G, Nguyen VT.
    Genomics; 1994 Sep 15; 23(2):331-7. PubMed ID: 7835881
    [Abstract] [Full Text] [Related]

  • 15. Mapping of short tandem repeat polymorphisms on human chromosome 3.
    Wilkie PJ, Weber JL.
    Genomics; 1994 Jan 01; 19(1):167-9. PubMed ID: 8188221
    [Abstract] [Full Text] [Related]

  • 16. Microsatellite polymorphism linkage map of human chromosome 13q.
    Bowcock A, Osborne-Lawrence S, Barnes R, Chakravarti A, Washington S, Dunn C.
    Genomics; 1993 Feb 01; 15(2):376-86. PubMed ID: 8095487
    [Abstract] [Full Text] [Related]

  • 17. A genetic analysis of the Werner syndrome region on human chromosome 8p.
    Thomas W, Rubenstein M, Goto M, Drayna D.
    Genomics; 1993 Jun 01; 16(3):685-90. PubMed ID: 8325642
    [Abstract] [Full Text] [Related]

  • 18. Linkage map of nine loci defined by polymorphic DNA markers assigned to rat chromosome 13.
    Remmers EF, Goldmuntz EA, Zha H, Mathern P, Du Y, Crofford LJ, Wilder RL.
    Genomics; 1993 Nov 01; 18(2):277-82. PubMed ID: 8288230
    [Abstract] [Full Text] [Related]

  • 19. A microsatellite-based multipoint index map of human chromosome 22.
    Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS.
    Genomics; 1993 Nov 01; 18(2):329-39. PubMed ID: 8288236
    [Abstract] [Full Text] [Related]

  • 20. Genetic and physical map of 11 short tandem repeat polymorphisms on human chromosome 6.
    Wilkie PJ, Polymeropoulos MH, Trent JM, Small KW, Weber JL.
    Genomics; 1993 Jan 01; 15(1):225-7. PubMed ID: 8432543
    [Abstract] [Full Text] [Related]

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