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Journal Abstract Search

205 related items for PubMed ID: 12557225

  • 21. High-resolution analysis of acquired genomic imbalances in bone marrow samples from chronic myeloid leukemia patients by use of multiple short DNA probes.
    Reid AG, Tarpey PS, Nacheva EP.
    Genes Chromosomes Cancer; 2003 Jul; 37(3):282-90. PubMed ID: 12759926
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  • 23. Cytogenetic, spectral karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization characterization of two new secondary leukemia cell lines with 5q deletions, and MYC and MLL amplification.
    Knutsen T, Pack S, Petropavlovskaja M, Padilla-Nash H, Knight C, Mickley LA, Ried T, Elwood PC, Roberts SJ.
    Genes Chromosomes Cancer; 2003 Jul; 37(3):270-81. PubMed ID: 12759925
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  • 24. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
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  • 25. Comparative genomic hybridization and multiplex-fluorescence in situ hybridization: an appraisal in elderly patients with acute myelogenous leukemia.
    Dalley CD, Neat MJ, Foot NJ, Burridge M, Byrne L, Amess JA, Rohatiner AZ, Lister A, Young BD, Lillington DM.
    Hematol J; 2002 Feb; 3(6):290-8. PubMed ID: 12522451
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  • 26. [Molecular cytogenetic analyses of patients with plasma cell myeloma in Tolna and Baranya counties in Hungary].
    Kosztolányi S, Horváth B, Hosnyánszki D, Kereskai L, Sziládi E, Jáksó P, Alizadeh H, Szuhai K, Alpár D, Kajtár B.
    Orv Hetil; 2019 Jun; 160(24):944-951. PubMed ID: 31433233
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  • 27. Genetic abnormalities detected by comparative genomic hybridization in a human endometriosis-derived cell line.
    Gogusev J, Bouquet de Jolinière J, Telvi L, Doussau M, du Manoir S, Stojkoski A, Levardon M.
    Mol Hum Reprod; 2000 Sep; 6(9):821-7. PubMed ID: 10956554
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  • 29. Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.
    Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H.
    Cytogenet Cell Genet; 2001 Sep; 93(3-4):188-94. PubMed ID: 11528111
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  • 30. Comparative genomic hybridization analysis identifies gains of 1p35 approximately p36 and chromosome 19 in osteosarcoma.
    Zielenska M, Bayani J, Pandita A, Toledo S, Marrano P, Andrade J, Petrilli A, Thorner P, Sorensen P, Squire JA.
    Cancer Genet Cytogenet; 2001 Oct 01; 130(1):14-21. PubMed ID: 11672768
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  • 32. [Combined use of molecular cytogenetic techniques to detect a small chromosomal translocation].
    Xie YJ, Chen BJ, Wu JZ, Chen Z, Lin SB, Fang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct 01; 28(5):568-71. PubMed ID: 21983737
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  • 34. Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome.
    Limon J, Nedoszytko B, Brozek I, Hellmann A, Zajaczek S, Lubiński J, Mrózek K.
    Cancer Genet Cytogenet; 1995 Aug 01; 83(1):75-81. PubMed ID: 7656210
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  • 35. Genetic characterization of Sézary's syndrome by conventional cytogenetics and cross-species color banding fluorescent in situhybridization.
    Espinet B, Salido M, Pujol RM, Florensa L, Gallardo F, Domingo A, Servitje O, Estrach T, Garcìa-Muret P, Woessner S, Serrano S, Solé F.
    Haematologica; 2004 Feb 01; 89(2):165-73. PubMed ID: 15003891
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  • 37. A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma.
    Strefford JC, Stasevich I, Lane TM, Lu YJ, Oliver T, Young BD.
    Cancer Genet Cytogenet; 2005 May 01; 159(1):1-9. PubMed ID: 15860350
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  • 39. Genomic alterations in blastic natural killer/extranodal natural killer-like T cell lymphoma with cutaneous involvement.
    Mao X, Onadim Z, Price EA, Child F, Lillington DM, Russell-Jones R, Young BD, Whittaker S.
    J Invest Dermatol; 2003 Sep 01; 121(3):618-27. PubMed ID: 12925224
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