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Journal Abstract Search

141 related items for PubMed ID: 2884625

  • 1.
    ; . PubMed ID:
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  • 2. Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.
    Lerman MI, Latif F, Glenn GM, Daniel LN, Brauch H, Hosoe S, Hampsch K, Delisio J, Orcutt ML, McBride OW.
    Hum Genet; 1991 Apr; 86(6):567-77. PubMed ID: 1673958
    [Abstract] [Full Text] [Related]

  • 3. A fine structure physical map of the short arm of chromosome 5.
    Overhauser J, Beaudet AL, Wasmuth JJ.
    Am J Hum Genet; 1986 Nov; 39(5):562-72. PubMed ID: 2878609
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  • 5. Isolation of polymorphic DNA fragments from human chromosome 4.
    Gilliam TC, Healey ST, MacDonald ME, Stewart GD, Wasmuth JJ, Tanzi RE, Roy JC, Gusella JF.
    Nucleic Acids Res; 1987 Feb 25; 15(4):1445-58. PubMed ID: 2881276
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  • 6. Isolation and analysis of DNA markers specific to human chromosome 15.
    Tasset DM, Hartz JA, Kao FT.
    Am J Hum Genet; 1988 Jun 25; 42(6):854-66. PubMed ID: 2897161
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  • 7. 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 25; 36(2):265-76. PubMed ID: 6324578
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  • 9. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
    Overhauser J, McMahon J, Oberlender S, Carlin ME, Niebuhr E, Wasmuth JJ, Lee-Chen J.
    Am J Med Genet; 1990 Sep 25; 37(1):83-6. PubMed ID: 1978567
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  • 10. Regional mapping of unique DNA sequences from human chromosome 3 derived from a flow-sorted chromosome library.
    Atchison LM, Naylor SL, Freed JJ, Comis RL.
    Cytogenet Cell Genet; 1988 Sep 25; 48(3):156-9. PubMed ID: 2906850
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  • 11. Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library.
    Stolz FM, Pfau HP, Reipen G, Schnittger S, Grzeschik KH, Hansmann I.
    Genomics; 1991 Dec 25; 11(4):948-55. PubMed ID: 1686021
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  • 12. Isolation and analysis of DNA marker revealing restriction fragment length polymorphism from X chromosome specific DNA library.
    Sadakane Y.
    Fukuoka Igaku Zasshi; 1989 Aug 25; 80(8):404-15. PubMed ID: 2573569
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  • 13. Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel.
    Jobs A, Klein-Bölting D, Jandel AS, Driesel A, Olek K, Grzeschik KH.
    Hum Genet; 1990 Jan 25; 84(2):147-50. PubMed ID: 1967587
    [Abstract] [Full Text] [Related]

  • 14. Construction of a map of the short arm of human chromosome 6.
    Leach R, DeMars R, Hasstedt S, White R.
    Proc Natl Acad Sci U S A; 1986 Jun 25; 83(11):3909-13. PubMed ID: 3012539
    [Abstract] [Full Text] [Related]

  • 15. Molecular genetics of human chromosome 4.
    Gusella JA, Gilliam TC, MacDonald ME, Cheng SV, Tanzi RE.
    J Med Genet; 1986 Jun 25; 23(3):193-9. PubMed ID: 2941587
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  • 16. Sixty-five radiation hybrids for the short arm of human chromosome 6: their value as a mapping panel and as a source for rapid isolation of new probes using repeat element-mediated PCR.
    Zoghbi HY, McCall AE, LeBorgne-Demarquoy F.
    Genomics; 1991 Apr 25; 9(4):713-20. PubMed ID: 1674731
    [Abstract] [Full Text] [Related]

  • 17. The X chromosome shows less genetic variation at restriction sites than the autosomes.
    Hofker MH, Skraastad MI, Bergen AA, Wapenaar MC, Bakker E, Millington-Ward A, van Ommen GJ, Pearson PL.
    Am J Hum Genet; 1986 Oct 25; 39(4):438-51. PubMed ID: 2876629
    [Abstract] [Full Text] [Related]

  • 18. Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).
    Wood S, Starr TV, Shukin RJ.
    Am J Hum Genet; 1986 Dec 25; 39(6):744-50. PubMed ID: 2879441
    [Abstract] [Full Text] [Related]

  • 19. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
    Nicholls RD, Knoll JH, Glatt K, Hersh JH, Brewster TD, Graham JM, Wurster-Hill D, Wharton R, Latt SA.
    Am J Med Genet; 1989 May 25; 33(1):66-77. PubMed ID: 2568752
    [Abstract] [Full Text] [Related]

  • 20. Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.
    Budarf ML, McDermid HE, Sellinger B, Emanuel BS.
    Genomics; 1991 Aug 25; 10(4):996-1002. PubMed ID: 1680800
    [Abstract] [Full Text] [Related]

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