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Journal Abstract Search

176 related items for PubMed ID: 1360193

  • 1. Linkage and association studies with C8A and C8B RFLPs on chromosome 1.
    Rogde S, Gedde-Dahl T, Teisberg P, Jonassen R, Høyheim B, Olaisen B.
    Ann Hum Genet; 1992 Jul; 56(3):233-42. PubMed ID: 1360193
    [Abstract] [Full Text] [Related]

  • 2. The C8A and C8B loci are closely linked on chromosome 1.
    Rogde S, Olaisen B, Gedde-Dahl T, Teisberg P.
    Ann Hum Genet; 1986 May; 50(2):139-44. PubMed ID: 3435043
    [Abstract] [Full Text] [Related]

  • 3. Chromosomal assignment of genes encoding the alpha, beta, and gamma subunits of human complement protein C8: identification of a close physical linkage between the alpha and the beta loci.
    Kaufman KM, Snider JV, Spurr NK, Schwartz CE, Sodetz JM.
    Genomics; 1989 Oct; 5(3):475-80. PubMed ID: 2613233
    [Abstract] [Full Text] [Related]

  • 4. DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes.
    Coto E, Martínez-Naves E, Domínguez O, DiScipio RG, Urra JM, López-Larrea C.
    Immunogenetics; 1991 Oct; 33(3):184-7. PubMed ID: 1672663
    [Abstract] [Full Text] [Related]

  • 5. Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.
    Zoghbi HY, Daiger SP, McCall A, O'Brien WE, Beaudet AL.
    Am J Hum Genet; 1988 Jun; 42(6):877-83. PubMed ID: 2897163
    [Abstract] [Full Text] [Related]

  • 6. Genetic control of the eighth component of complement.
    Raum D, Spence MA, Balavitch D, Tideman S, Merritt AD, Taggart RT, Petersen BH, Day NK, Alper CA.
    J Clin Invest; 1979 Sep; 64(3):858-65. PubMed ID: 468996
    [Abstract] [Full Text] [Related]

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  • 8. Genetic basis of human complement C8 beta deficiency.
    Kaufmann T, Hänsch G, Rittner C, Späth P, Tedesco F, Schneider PM.
    J Immunol; 1993 Jun 01; 150(11):4943-7. PubMed ID: 8098723
    [Abstract] [Full Text] [Related]

  • 9. Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.
    MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG.
    Am J Hum Genet; 1989 Jan 01; 44(1):140-7. PubMed ID: 2562820
    [Abstract] [Full Text] [Related]

  • 10. Multilocus linkage analysis with the human argininosuccinate synthetase gene.
    Northrup H, Lathrop M, Lu SY, Daiger SP, Beaudet AL, O'Brien WE.
    Genomics; 1989 Oct 01; 5(3):442-4. PubMed ID: 2575581
    [Abstract] [Full Text] [Related]

  • 11. Polymorphism of the complement C8A and -B genes in two families with C8 beta deficiency and neisserial infections.
    Barba GM, Kaufmann TJ, Schneider PM, Rittner C, Brai M.
    Clin Immunol Immunopathol; 1994 Jul 01; 72(1):83-9. PubMed ID: 8020197
    [Abstract] [Full Text] [Related]

  • 12. Genetic aspects of complement component C8 in Norwegian meningococcal disease patients.
    Rogde S, Høiby EA, Teisberg P, Olaisen B.
    Scand J Infect Dis; 1990 Jul 01; 22(6):673-9. PubMed ID: 2284574
    [Abstract] [Full Text] [Related]

  • 13. A BamHI RFLP of the C8A gene.
    Rogde S, Olaisen B, Teisberg P, Sodetz J.
    Nucleic Acids Res; 1991 Jul 11; 19(13):3762. PubMed ID: 1677187
    [No Abstract] [Full Text] [Related]

  • 14. Genetic linkage map of human chromosome 21.
    Tanzi RE, Haines JL, Watkins PC, Stewart GD, Wallace MR, Hallewell R, Wong C, Wexler NS, Conneally PM, Gusella JF.
    Genomics; 1988 Aug 11; 3(2):129-36. PubMed ID: 2906323
    [Abstract] [Full Text] [Related]

  • 15. Genetic linkage heterogeneity in the fragile X syndrome.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Hum Genet; 1985 Aug 11; 71(1):11-8. PubMed ID: 2993154
    [Abstract] [Full Text] [Related]

  • 16. Adult polycystic kidney disease and linked RFLPs at the alpha globin locus: a genetic study in the South Wales population.
    Lazarou LP, Davies F, Sarfarazi M, Coles GA, Harper PS.
    J Med Genet; 1987 Aug 11; 24(8):466-73. PubMed ID: 2443703
    [Abstract] [Full Text] [Related]

  • 17. Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis.
    Maher ER, Bentley E, Yates JR, Barton D, Jennings A, Fellows IW, Ponder MA, Ponder BA, Benjamin C, Harris R.
    J Neurol Sci; 1990 Dec 11; 100(1-2):27-30. PubMed ID: 1982450
    [Abstract] [Full Text] [Related]

  • 18. The human complement C8G gene, a member of the lipocalin gene family: polymorphisms and mapping to chromosome 9q34.3.
    Dewald G, Cichon S, Bryant SP, Hemmer S, Nöthen MM, Spurr NK.
    Ann Hum Genet; 1996 Jul 11; 60(4):281-91. PubMed ID: 8865989
    [Abstract] [Full Text] [Related]

  • 19. Chromosomal assignment and physical linkage of the human C8 loci: implications regarding C8 polymorphisms and deficiencies.
    Snider JV, Kaufman KM, Sodetz JM.
    Complement Inflamm; 1990 Jul 11; 7(4-6):298-301. PubMed ID: 2088669
    [Abstract] [Full Text] [Related]

  • 20. Allelic association and linkage studies in Wilson disease.
    Thomas GR, Roberts EA, Rosales TO, Moroz SP, Lambert MA, Wong LT, Cox DW.
    Hum Mol Genet; 1993 Sep 11; 2(9):1401-5. PubMed ID: 7902160
    [Abstract] [Full Text] [Related]

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