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 *

146 related articles for article (PubMed ID: 6286461)

  • 1. The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.
    Hill ME; Davies KE; Harper P; Williamson R
    Hum Genet; 1982; 60(3):222-6. PubMed ID: 6286461
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.
    Page D; de Martinville B; Barker D; Wyman A; White R; Francke U; Botstein D
    Proc Natl Acad Sci U S A; 1982 Sep; 79(17):5352-6. PubMed ID: 6291041
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis of genetic disease using recombinant DNA.
    Cooper DN; Schmidtke J
    Hum Genet; 1986 May; 73(1):1-11. PubMed ID: 3011642
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Linkage studies of polymorphic, repeated DNA sequences in centromeric regions of human chromosomes.
    Jabs EW; Meyers DA; Bias WB
    Am J Hum Genet; 1986 Mar; 38(3):297-308. PubMed ID: 3006481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.
    Wieacker P; Davies KE; Cooke HJ; Pearson PL; Williamson R; Bhattacharya S; Zimmer J; Ropers HH
    Am J Hum Genet; 1984 Mar; 36(2):265-76. PubMed ID: 6324578
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).
    Trent JM; Flink IL; Morkin E; van Tuinen P; Ledbetter DH
    Am J Hum Genet; 1987 Sep; 41(3):428-35. PubMed ID: 3115094
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome.
    Wieacker P; Davies KE; Mevorah B; Ropers HH
    Hum Genet; 1983; 63(2):113-6. PubMed ID: 6301973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome.
    Brown CS; Pearson PL; Thomas NS; Sarfarazi M; Harper PS; Shaw DJ
    J Med Genet; 1985 Jun; 22(3):179-81. PubMed ID: 2989525
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.
    Roncuzzi L; Fadda S; Mochi M; Prosperi L; Sangiorgi S; Santamaria R; Sbarra D; Besana D; Morandi L; Rocchi M
    Am J Hum Genet; 1985 Mar; 37(2):407-17. PubMed ID: 2984927
    [TBL] [Abstract][Full Text] [Related]  

  • 10. DNA polymorphism of the RC8 probe on the X-chromosome. Identification of a new DNA variant with the TaqI enzyme.
    Børresen AL; Jordfald AB; Berg K
    Clin Genet; 1985 Apr; 27(4):411-3. PubMed ID: 2986884
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus.
    Scheffer H; van der Lelie D; Aanstoot GH; Goor N; Nienhaus AJ; van der Hout AH; Pearson PL; Buys CH
    Hum Genet; 1986 Nov; 74(3):249-55. PubMed ID: 2877932
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.
    Gal A; Mücke J; Theile H; Wieacker PF; Ropers HH; Wienker TF
    Hum Genet; 1985; 70(1):38-42. PubMed ID: 2987105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Sequences homologous to the human D1S1 locus present on human chromosome 3.
    Carritt B; Welch HM; Parry-Jones NJ
    Am J Hum Genet; 1986 Apr; 38(4):428-36. PubMed ID: 3010709
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.
    Bleeker-Wagemakers LM; Friedrich U; Gal A; Wienker TF; Warburg M; Ropers HH
    Hum Genet; 1985; 71(3):211-4. PubMed ID: 2998969
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A strategy to reveal high-frequency RFLPs along the human X chromosome.
    Aldridge J; Kunkel L; Bruns G; Tantravahi U; Lalande M; Brewster T; Moreau E; Wilson M; Bromley W; Roderick T
    Am J Hum Genet; 1984 May; 36(3):546-64. PubMed ID: 6328976
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation and analysis of DNA marker revealing restriction fragment length polymorphism from X chromosome specific DNA library.
    Sadakane Y
    Fukuoka Igaku Zasshi; 1989 Aug; 80(8):404-15. PubMed ID: 2573569
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.
    Oberlé I; Drayna D; Camerino G; White R; Mandel JL
    Proc Natl Acad Sci U S A; 1985 May; 82(9):2824-8. PubMed ID: 2986139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26----qter.
    Boggs BA; Nussbaum RL
    Somat Cell Mol Genet; 1984 Nov; 10(6):607-13. PubMed ID: 6095463
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.
    Brown CJ; Goss SJ; Lubahn DB; Joseph DR; Wilson EM; French FS; Willard HF
    Am J Hum Genet; 1989 Feb; 44(2):264-9. PubMed ID: 2563196
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
    Hofker MH; Bergen AA; Skraastad MI; Carpenter NJ; Veenema H; Connor JM; Bakker E; van Ommen GJ; Pearson PL
    Am J Hum Genet; 1987 Apr; 40(4):312-28. PubMed ID: 2883888
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.