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Journal Abstract Search

150 related items for PubMed ID: 2004552

  • 1. Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes.
    Lengauer C, Eckelt A, Weith A, Endlich N, Ponelies N, Lichter P, Greulich KO, Cremer T.
    Cytogenet Cell Genet; 1991; 56(1):27-30. PubMed ID: 2004552
    [Abstract] [Full Text] [Related]

  • 2. Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probe.
    Trautmann U, Leuteritz G, Senger G, Claussen U, Ballhausen WG.
    Hum Genet; 1991 Aug; 87(4):495-7. PubMed ID: 1652549
    [Abstract] [Full Text] [Related]

  • 3. [Selective chromosome painting using in situ hybridization].
    Pérez Losada A, Woessner S, Solé F, Caballín MR, Florensa L.
    Sangre (Barc); 1993 Apr; 38(2):151-4. PubMed ID: 8516730
    [Abstract] [Full Text] [Related]

  • 4. Direct microdissection and microcloning of a translocation breakpoint region, t(1;11)(q42.2;q21), associated with schizophrenia.
    Muir WJ, Gosden CM, Brookes AJ, Fantes J, Evans KL, Maguire SM, Stevenson B, Boyle S, Blackwood DH, St Clair DM.
    Cytogenet Cell Genet; 1995 Apr; 70(1-2):35-40. PubMed ID: 7736785
    [Abstract] [Full Text] [Related]

  • 5. Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool.
    Deng HX, Yoshiura K, Dirks RW, Harada N, Hirota T, Tsukamoto K, Jinno Y, Niikawa N.
    Hum Genet; 1992 Apr; 89(1):13-7. PubMed ID: 1577461
    [Abstract] [Full Text] [Related]

  • 6. Characterization of marker chromosomes in Namalva cells by chromosomal in situ suppression (CISS) hybridization and R-banding.
    Ruppersberger P, Arnold M, Zankl H, Scherthan H.
    Genes Chromosomes Cancer; 1991 Sep; 3(5):394-9. PubMed ID: 1797087
    [Abstract] [Full Text] [Related]

  • 7. Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.
    Lengauer C, Riethman HC, Speicher MR, Taniwaki M, Konecki D, Green ED, Becher R, Olson MV, Cremer T.
    Cancer Res; 1992 May 01; 52(9):2590-6. PubMed ID: 1568226
    [Abstract] [Full Text] [Related]

  • 8. Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization.
    Cremer T, Popp S, Emmerich P, Lichter P, Cremer C.
    Cytometry; 1990 May 01; 11(1):110-8. PubMed ID: 2307051
    [Abstract] [Full Text] [Related]

  • 9. Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
    Liehr T, Weise A, Heller A, Starke H, Mrasek K, Kuechler A, Weier HU, Claussen U.
    Cytogenet Genome Res; 2002 May 01; 97(1-2):43-50. PubMed ID: 12438737
    [Abstract] [Full Text] [Related]

  • 10. Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.
    Jauch A, Daumer C, Lichter P, Murken J, Schroeder-Kurth T, Cremer T.
    Hum Genet; 1990 Jul 01; 85(2):145-50. PubMed ID: 2370043
    [Abstract] [Full Text] [Related]

  • 11. Large-scale isolation of human 1p36-specific P1 clones and their use for fluorescence in situ hybridization.
    Lengauer C, Henn T, Onyango P, Francis F, Lehrach H, Weith A.
    Genet Anal Tech Appl; 1994 Jul 01; 11(5-6):140-7. PubMed ID: 7710779
    [Abstract] [Full Text] [Related]

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  • 13. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique].
    Pérez Losada A, Solé F, Woessner S, Florensa L, Besses C, Espinet B, Caballín MR, García Eroles L, Sans-Sabrafén J.
    Sangre (Barc); 1996 Jun 01; 41(3):201-9. PubMed ID: 8755208
    [Abstract] [Full Text] [Related]

  • 14. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.
    Lichter P, Cremer T, Borden J, Manuelidis L, Ward DC.
    Hum Genet; 1988 Nov 01; 80(3):224-34. PubMed ID: 3192212
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  • 16. Chromosome in situ suppression hybridisation in clinical cytogenetics.
    Hulten MA, Gould CP, Goldman AS, Waters JJ.
    J Med Genet; 1991 Sep 01; 28(9):577-82. PubMed ID: 1956055
    [Abstract] [Full Text] [Related]

  • 17. Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
    Sullivan BA, Leana-Cox J, Schwartz S.
    Am J Med Genet; 1993 Aug 15; 47(2):223-30. PubMed ID: 8213910
    [Abstract] [Full Text] [Related]

  • 18. Simultaneous detection of centromere-specific probes and chromosome painting libraries by a combination of primed in situ labelling and chromosome painting (PRINS-painting).
    Hindkjaer J, Brandt CA, Koch J, Lund TB, Kølvraa S, Bolund L.
    Chromosome Res; 1995 Jan 15; 3(1):41-4. PubMed ID: 7704414
    [Abstract] [Full Text] [Related]

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  • 20. [Molecular cytogenetic detection of minute chromosomal structural abnormality on the chromosomal terminal regions].
    Tan YQ, Li LY, Lu GX.
    Yi Chuan Xue Bao; 2002 Sep 15; 29(9):753-6. PubMed ID: 12561219
    [Abstract] [Full Text] [Related]

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