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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 6286461)

  • 41. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE; Mattei MG; Mattei JF; Veenema H; McGlade S; Harper K; Tommerup N; Nielsen KB; Mikkelsen M; Beighton P
    Hum Genet; 1985; 70(3):249-55. PubMed ID: 2991115
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A restriction-fragment-length difference detected by the anonymous probe DXS199 exhibits non-Mendelian inheritance.
    Starr T; Wood S
    Am J Hum Genet; 1988 Feb; 42(2):267-70. PubMed ID: 2893545
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Isolation of polymorphic DNA segments from human chromosome 21.
    Watkins PC; Tanzi RE; Gibbons KT; Tricoli JV; Landes G; Eddy R; Shows TB; Gusella JF
    Nucleic Acids Res; 1985 Sep; 13(17):6075-88. PubMed ID: 4047940
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A highly polymorphic locus in human DNA.
    Wyman AR; White R
    Proc Natl Acad Sci U S A; 1980 Nov; 77(11):6754-8. PubMed ID: 6935681
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Localization of a human heat-shock HSP 70 gene sequence to chromosome 6 and detection of two other loci by somatic-cell hybrid and restriction fragment length polymorphism analysis.
    Goate AM; Cooper DN; Hall C; Leung TK; Solomon E; Lim L
    Hum Genet; 1987 Feb; 75(2):123-8. PubMed ID: 2880793
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps.
    Willard HF; Waye JS; Skolnick MH; Schwartz CE; Powers VE; England SB
    Proc Natl Acad Sci U S A; 1986 Aug; 83(15):5611-5. PubMed ID: 3016709
    [TBL] [Abstract][Full Text] [Related]  

  • 47. New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
    Schnur RE; Ledbetter SA; Ledbetter DH; Merry DE; Nussbaum RL
    Am J Hum Genet; 1989 Feb; 44(2):248-54. PubMed ID: 2563194
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Mapping X-linked ophthalmic diseases. Provisional assignment of the locus for choroideremia to Xq13-q24.
    Lewis RA; Nussbaum RL; Ferrell R
    Ophthalmology; 1985 Jun; 92(6):800-6. PubMed ID: 4034175
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
    Botstein D; White RL; Skolnick M; Davis RW
    Am J Hum Genet; 1980 May; 32(3):314-31. PubMed ID: 6247908
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci.
    Kunkel LM; Lalande M; Monaco AP; Flint A; Middlesworth W; Latt SA
    Gene; 1985; 33(3):251-8. PubMed ID: 2989089
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Localization of the hydroxyindole-O-methyltransferase gene to the pseudoautosomal region: implications for mapping of psychiatric disorders.
    Yi H; Donohue SJ; Klein DC; McBride OW
    Hum Mol Genet; 1993 Feb; 2(2):127-31. PubMed ID: 8098975
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
    Kingston HM; Thomas NS; Pearson PL; Sarfarazi M; Harper PS
    J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Molecular analysis of females manifesting thyroxine-binding globulin (TBG) deficiency: selective X-chromosome inactivation responsible for the difference between phenotype and genotype in TBG-deficient females.
    Okamoto H; Mori Y; Tani Y; Nakagomi Y; Sano T; Ohyama K; Saito H; Oiso Y
    J Clin Endocrinol Metab; 1996 Jun; 81(6):2204-8. PubMed ID: 8964852
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Elevated thyroxine-binding globulin with X-chromosome linked inheritance.
    Buchanan BD; Hagen GA
    Clin Endocrinol (Oxf); 1979 Dec; 11(6):665-9. PubMed ID: 119595
    [TBL] [Abstract][Full Text] [Related]  

  • 55. DNA polymorphic haplotypes on the short arm of chromosome 11 and the inheritance of type I diabetes mellitus.
    Ferns GA; Hitman GA; Trembath R; Williams L; Tarn A; Gale EA; Galton DJ
    J Med Genet; 1986 Jun; 23(3):210-6. PubMed ID: 3014147
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid.
    Litt M; Sheehy R; Bruns GA; Magenis RE
    Hum Genet; 1986 Aug; 73(4):340-5. PubMed ID: 3017843
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.
    Kwan SP; Kunkel L; Bruns G; Wedgwood RJ; Latt S; Rosen FS
    J Clin Invest; 1986 Feb; 77(2):649-52. PubMed ID: 3003164
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A hypervariable repeated sequence on human chromosome 1p36.
    Buroker N; Bestwick R; Haight G; Magenis RE; Litt M
    Hum Genet; 1987 Oct; 77(2):175-81. PubMed ID: 2888721
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24.
    Baas F; Bikker H; Geurts van Kessel A; Melsert R; Pearson PL; de Vijlder JJ; van Ommen GJ
    Hum Genet; 1985; 69(2):138-43. PubMed ID: 2982724
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes.
    Ramesh V; Eddy R; Bruns GA; Shih VE; Shows TB; Gusella JF
    Hum Genet; 1987 Jun; 76(2):121-6. PubMed ID: 2886418
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.