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Journal Abstract Search

141 related items for PubMed ID: 1958589

  • 1. Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes.
    Smit VT, Wessels JW, Mollevanger P, Dauwerse JG, van Vliet M, Beverstock GC, Breuning MH, Devilee P, Raap AK, Cornelisse CJ.
    Genes Chromosomes Cancer; 1991 Jul; 3(4):239-48. PubMed ID: 1958589
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  • 7. Homologies in human and Macaca fuscata chromosomes revealed by in situ suppression hybridization with human chromosome specific DNA libraries.
    Wienberg J, Stanyon R, Jauch A, Cremer T.
    Chromosoma; 1992 Mar; 101(5-6):265-70. PubMed ID: 1576879
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  • 8. Chromosome painting as a supplement to cytogenetic banding analysis in non-Hodgkin's lymphoma.
    Bajalica S, Sørensen AG, Pedersen NT, Heim S, Brøndum-Nielsen K.
    Genes Chromosomes Cancer; 1993 Aug; 7(4):231-9. PubMed ID: 7692950
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  • 9. Fluorescence in situ hybridization analysis using cosmid probes to define chromosome 6q abnormalities in ovarian carcinoma cell lines.
    Lastowska MA, Lillington DM, Shelling AN, Cooke I, Gibbons B, Young BD, Ganesan TS.
    Cancer Genet Cytogenet; 1994 Oct 15; 77(2):99-105. PubMed ID: 7954328
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  • 12. Molecular localization of the t(11;22)(q24;q12) translocation of Ewing sarcoma by chromosomal in situ suppression hybridization.
    Selleri L, Hermanson GG, Eubanks JH, Lewis KA, Evans GA.
    Proc Natl Acad Sci U S A; 1991 Feb 01; 88(3):887-91. PubMed ID: 1992479
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  • 15. [The use of DNA hybridization in situ for identifying chromosomal rearrangements in the karyotyping of cell lines].
    Grabovskaia IL, Glukhova LA, Tsevtkova TG, Kravets IA, Mamaeva SE, Kushch AA.
    Tsitologiia; 1992 Feb 01; 34(7):41-6. PubMed ID: 1335625
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  • 16. Combined Q-banding and fluorescence in situ hybridization for the identification of bovine chromosomes 1 to 7.
    Solinas-Toldo S, Mezzelani A, Hawkins GA, Bishop MD, Olsaker I, Mackinlay A, Ferretti L, Fries R.
    Cytogenet Cell Genet; 1995 Feb 01; 69(1-2):1-6. PubMed ID: 7835074
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  • 18. Molecular cytogenetic analysis of non-small cell lung carcinoma by spectral karyotyping and comparative genomic hybridization.
    Luk C, Tsao MS, Bayani J, Shepherd F, Squire JA.
    Cancer Genet Cytogenet; 2001 Mar 01; 125(2):87-99. PubMed ID: 11369051
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  • 19. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.
    du Manoir S, Speicher MR, Joos S, Schröck E, Popp S, Döhner H, Kovacs G, Robert-Nicoud M, Lichter P, Cremer T.
    Hum Genet; 1993 Feb 01; 90(6):590-610. PubMed ID: 8444465
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  • 20. 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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