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

87 related items for PubMed ID: 7836855

  • 21. Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families.
    Watts GD, O'Briant KC, Chance PF.
    Hum Genet; 2002 Feb; 110(2):166-72. PubMed ID: 11935323
    [Abstract] [Full Text] [Related]

  • 22. Heterologous mitochondrial DNA recombination in human cells.
    D'Aurelio M, Gajewski CD, Lin MT, Mauck WM, Shao LZ, Lenaz G, Moraes CT, Manfredi G.
    Hum Mol Genet; 2004 Dec 15; 13(24):3171-9. PubMed ID: 15496432
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Vitamin D receptor: no evidence for allele-specific mRNA stability in cells which are heterozygous for the Taq I restriction enzyme polymorphism.
    Verbeek W, Gombart AF, Shiohara M, Campbell M, Koeffler HP.
    Biochem Biophys Res Commun; 1997 Sep 08; 238(1):77-80. PubMed ID: 9299455
    [Abstract] [Full Text] [Related]

  • 25. PCR detection of the Taq1 restriction fragment length polymorphism linked to the ataxia telangiectasia locus.
    Athma P, Liu J, Swift M.
    Clin Chem; 1995 Apr 08; 41(4):625-6. PubMed ID: 7720261
    [No Abstract] [Full Text] [Related]

  • 26. A family showing no evidence of linkage between the ataxia telangiectasia gene and chromosome 11q22-23.
    Hernandez D, McConville CM, Stacey M, Woods CG, Brown MM, Shutt P, Rysiecki G, Taylor AM.
    J Med Genet; 1993 Feb 08; 30(2):135-40. PubMed ID: 8445618
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Ataxia-telangiectasia in Italy: genetic analysis.
    Chessa L, Lisa A, Fiorani O, Zei G.
    Int J Radiat Biol; 1994 Dec 08; 66(6 Suppl):S31-3. PubMed ID: 7836850
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Detection of a frequent restriction fragment length polymorphism in the human T cell antigen receptor beta chain locus. A potential diagnostic tool.
    Berliner N, Duby AD, Morton CC, Leder P, Seidman JG.
    J Clin Invest; 1985 Sep 08; 76(3):1283-5. PubMed ID: 2995449
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes.
    Sirugo G, Keats B, Fujita R, Duclos F, Purohit K, Koenig M, Mandel JL.
    Am J Hum Genet; 1992 Mar 08; 50(3):559-66. PubMed ID: 1347194
    [Abstract] [Full Text] [Related]

  • 34. D20S16 is a complex interspersed repeated sequence: genetic and physical analysis of the locus.
    Bowden DW, Krawchuk MD, Weaver EJ, Howard TD, Knowlton RG, Rao PN, Pettenati MJ, Hayworth R, Wagner BJ, Rothschild CB.
    Genomics; 1995 Jan 20; 25(2):394-403. PubMed ID: 7789973
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. [DNA polymorphism and genetic diseases].
    Baiget M.
    Med Clin (Barc); 1986 May 10; 86(18):774-7. PubMed ID: 3526011
    [No Abstract] [Full Text] [Related]

  • 37. A TaqI site identifies the *A allele at the ACP1 locus.
    Sensabaugh GF, Lazaruk KA.
    Hum Mol Genet; 1993 Jul 10; 2(7):1079. PubMed ID: 8364553
    [No Abstract] [Full Text] [Related]

  • 38. Detection of novel genetic markers by mismatch analysis.
    Roberts RG, Montandon AJ, Bobrow M, Bentley DR.
    Nucleic Acids Res; 1989 Aug 11; 17(15):5961-71. PubMed ID: 2570401
    [Abstract] [Full Text] [Related]

  • 39. Considerations affecting the feasibility of mapping a single-gene disorder using restriction fragment polymorphisms, with special reference to ataxia-telangiectasia.
    Botstein D.
    Kroc Found Ser; 1985 Aug 11; 19():125-31. PubMed ID: 3864934
    [No Abstract] [Full Text] [Related]

  • 40. A new polymorphic probe on chromosome 3p: lambda LIB15-44 (D3S596).
    Latif F, Glenn GM, Brauch H, Delisio J, Hampsch K, Orcutt ML, Zbar B, Lerman MI.
    Nucleic Acids Res; 1991 Feb 25; 19(4):965. PubMed ID: 2017384
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 5.