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Journal Abstract Search

181 related items for PubMed ID: 7529547

  • 1. Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.
    Schoenmakers EF, Mols R, Wanschura S, Kools PF, Geurts JM, Bartnitzke S, Bullerdiek J, van den Berghe H, Van de Ven WJ.
    Genes Chromosomes Cancer; 1994 Oct; 11(2):106-18. PubMed ID: 7529547
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  • 2. Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma.
    Schoenmakers EF, Kools PF, Mols R, Kazmierczak B, Bartnitzke S, Bullerdiek J, Dal Cin P, De Jong PJ, Van den Berghe H, Van de Ven WJ.
    Genomics; 1994 Mar 15; 20(2):210-22. PubMed ID: 8020967
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  • 3. A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.
    Schoenmakers EF, Geurts JM, Kools PF, Mols R, Huysmans C, Bullerdiek J, Van den Berghe H, Van de Ven WJ.
    Genomics; 1995 Oct 10; 29(3):665-78. PubMed ID: 8575759
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  • 4. Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma.
    Bhugra B, Smolarek TA, Lynch RA, Meloni AM, Sandberg AA, Deaven L, Menon AG.
    Cancer Lett; 1998 Apr 24; 126(2):119-26. PubMed ID: 9585056
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  • 5. Molecular-cytogenetic refinement of the 12q14-->q15 breakpoint region affected in uterine leiomyomas.
    Wanschura S, Hennig Y, Deichert U, Schoenmakers EF, Van de Ven WJ, Bartnitzke S, Bullerdiek J.
    Cytogenet Cell Genet; 1995 Apr 24; 71(2):131-5. PubMed ID: 7656581
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  • 6. Identification of the chromosome 12 translocation breakpoint region of a pleomorphic salivary gland adenoma with t(1;12)(p22;q15) as the sole cytogenetic abnormality.
    Kools PF, Wanschura S, Schoenmakers EF, Geurts JM, Mols R, Kazmierczak B, Bullerdiek J, Van den Berghe H, Van de Ven WJ.
    Cancer Genet Cytogenet; 1995 Jan 24; 79(1):1-7. PubMed ID: 7850744
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  • 13. Physical mapping of the uterine leiomyoma t(12;14)(q13-15;q24.1) breakpoint on chromosome 14 between SPTB and D14S77.
    Hug K, Doney MK, Tyler MJ, Grundy DA, Soukup S, Houseal TW, Menon AG.
    Genes Chromosomes Cancer; 1994 Dec 24; 11(4):263-6. PubMed ID: 7533530
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  • 15. Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15.
    Quade BJ, Weremowicz S, Neskey DM, Vanni R, Ladd C, Dal Cin P, Morton CC.
    Cancer Res; 2003 Mar 15; 63(6):1351-8. PubMed ID: 12649198
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  • 16. Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540.
    Doney MK, Gerken SC, Lynch R, Bhugra B, Hug K, White R, Weissenbach J, Menon AG.
    Cancer Lett; 1995 Sep 25; 96(2):245-52. PubMed ID: 7585464
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  • 20. Detection of chromosomal abnormalities of chromosome 12 in uterine leiomyoma using fluorescence in situ hybridization.
    Hayashi S, Miharu N, Okamoto E, Samura O, Hara T, Ohama K.
    Jpn J Hum Genet; 1996 Mar 25; 41(1):193-202. PubMed ID: 8914635
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