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Journal Abstract Search

147 related items for 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
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  • 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
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  • 3. Diagnosis of genetic disease using recombinant DNA.
    Cooper DN, Schmidtke J.
    Hum Genet; 1986 May; 73(1):1-11. PubMed ID: 3011642
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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 Mar; 71(3):211-4. PubMed ID: 2998969
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  • 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
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