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Journal Abstract Search

392 related items for PubMed ID: 2882953

  • 1. Localization and linkage of three polymorphic DNA sequences on human chromosome 20.
    Goodfellow PJ, Duncan AM, Farrer LA, Holden JJ, White BN, Kidd JR, Kidd KK, Simpson NE.
    Cytogenet Cell Genet; 1987; 44(2-3):112-7. PubMed ID: 2882953
    [Abstract] [Full Text] [Related]

  • 2. The polymorphic DNA sequence D20S14 is assigned to human chromosome 20p12----p11.2 by in situ hybridization.
    Löffler C, Rao VV, Hansmann I.
    Cytogenet Cell Genet; 1992; 59(1):20-1. PubMed ID: 1733666
    [Abstract] [Full Text] [Related]

  • 3. Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against synteny.
    Farrer LA, Goodfellow PJ, White BN, Holden JJ, Kidd JR, Simpson NE, Kidd KK.
    Cancer Genet Cytogenet; 1987 Aug; 27(2):327-34. PubMed ID: 2885081
    [Abstract] [Full Text] [Related]

  • 4. Linkage relationships of human arginine vasopressin-neurophysin-II and oxytocin-neurophysin-I to prodynorphin and other loci on chromosome 20.
    Summar ML, Phillips JA, Battey J, Castiglione CM, Kidd KK, Maness KJ, Weiffenbach B, Gravius TC.
    Mol Endocrinol; 1990 Jun; 4(6):947-50. PubMed ID: 1978246
    [Abstract] [Full Text] [Related]

  • 5. Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.
    Goodfellow PJ, White BN, Holden JJ, Duncan AM, Sears EV, Wang HS, Berlin L, Kidd KK, Simpson NE.
    Am J Hum Genet; 1985 Sep; 37(5):890-7. PubMed ID: 2864854
    [Abstract] [Full Text] [Related]

  • 6. The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.
    Wu JS, Giuffra LA, Goodfellow PJ, Myers S, Carson NL, Anderson L, Hoyle LS, Simpson NE, Kidd KK.
    Hum Genet; 1989 Nov; 83(4):383-90. PubMed ID: 2572537
    [Abstract] [Full Text] [Related]

  • 7. A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.
    Hazan J, Dubay C, Pankowiak MP, Becuwe N, Weissenbach J.
    Genomics; 1992 Feb; 12(2):183-9. PubMed ID: 1740328
    [Abstract] [Full Text] [Related]

  • 8. A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3.
    Yamakawa K, Morita R, Takahashi E, Hori T, Lathrop M, Nakamura Y.
    Genomics; 1991 Nov; 11(3):565-72. PubMed ID: 1685476
    [Abstract] [Full Text] [Related]

  • 9. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
    Arveiler B, Oberlé I, Mandel JL.
    Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
    [Abstract] [Full Text] [Related]

  • 10. Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18.
    Müller U, Donlon TA, Harris P, Rose E, Hoffman E, Bruns GP, Latt SA.
    Cytogenet Cell Genet; 1987 Sep; 45(1):16-20. PubMed ID: 2885151
    [Abstract] [Full Text] [Related]

  • 11. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.
    Bufton L, Bruns GA, Magenis RE, Tomar D, Shaw D, Brook D, Litt M.
    Am J Hum Genet; 1986 Apr; 38(4):447-60. PubMed ID: 3010711
    [Abstract] [Full Text] [Related]

  • 12. Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization.
    Magenis RE, Gusella J, Weliky K, Olson S, Haight G, Toth-Fejel S, Sheehy R.
    Am J Hum Genet; 1986 Sep; 39(3):383-91. PubMed ID: 2876628
    [Abstract] [Full Text] [Related]

  • 13. Regional localization by in situ hybridization of a human chromosome 9 marker tightly linked to the Friedreich's ataxia locus.
    Raimondi E, Antonelli A, Driesel AJ, Pandolfo M.
    Hum Genet; 1990 Jun; 85(1):125-6. PubMed ID: 1972693
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Mapping of seven polymorphic loci on human chromosome 13 by in situ hybridization.
    Dryja TP, Morton CC.
    Hum Genet; 1985 Oct; 71(3):192-5. PubMed ID: 4065891
    [Abstract] [Full Text] [Related]

  • 16. Diastrophic dysplasia gene maps to the distal long arm of chromosome 5.
    Hästbacka J, Kaitila I, Sistonen P, de la Chapelle A.
    Proc Natl Acad Sci U S A; 1990 Oct; 87(20):8056-9. PubMed ID: 1978318
    [Abstract] [Full Text] [Related]

  • 17. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
    Bowcock AM, Farrer LA, Cavalli-Sforza LL, Hebert JM, Kidd KK, Frydman M, Bonne-Tamir B.
    Am J Hum Genet; 1987 Jul; 41(1):27-35. PubMed ID: 3474893
    [Abstract] [Full Text] [Related]

  • 18. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.
    Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS.
    Genomics; 1988 Jul; 3(1):39-43. PubMed ID: 2906042
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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