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Journal Abstract Search

124 related items for PubMed ID: 17490536

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  • 3. [Detection of abnormal numbers of chromosome 8 with interphase fluorescence in situ hybridization in hematologic malignancies].
    Wang HP, Li GX, Qiao ZH, Wang HW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):395-7. PubMed ID: 15300644
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  • 4. Fluorescence in situ hybridization for the detection of trisomies 8 and 9 in polycythemia vera.
    Amiel A, Gaber E, Manor Y, Fejgin M, Joseph-Lerner N, Ravid M, Lishner M.
    Cancer Genet Cytogenet; 1995 Feb; 79(2):153-6. PubMed ID: 7889510
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  • 5. [Detection of trisomy 8 with interphase fluorescence in situ hybridization in myelodysplastic syndromes].
    Li J, Pan J, Xue Y, Wu C, Xie X, Guo Y, Ruan C.
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):179-81. PubMed ID: 11876976
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  • 7. The detection of trisomies 8 and 9 in patients with essential thrombocytosis by fluorescence in situ hybridization.
    Elis A, Amiel A, Manor Y, Tangi I, Fejgin M, Lishner M.
    Cancer Genet Cytogenet; 1996 Nov; 92(1):14-7. PubMed ID: 8956864
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  • 8. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V, Castagné C, Mühlematter D, Parlier V, Gmür J, Hess U, Kovacsovics T, Meyer-Monard S, Tichelli A, Tobler A, Jacky E, Schanz U, Bargetzi M, Hagemeijer A, de Witte T, van Melle G, Jotterand M.
    Cancer Genet Cytogenet; 2004 Jul 01; 152(1):29-41. PubMed ID: 15193439
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  • 9. Conventional and molecular cytogenetic features of myelodysplastic syndrome in China.
    Chen L, Li J, Zhu Y, Qiu H, Pan J, Wang R, Qian S, Xu W, Xue Y.
    Exp Oncol; 2007 Dec 01; 29(4):299-303. PubMed ID: 18199987
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  • 10. Exploring polycythaemia vera with fluorescence in situ hybridization: additional cryptic 9p is the most frequent abnormality detected.
    Najfeld V, Montella L, Scalise A, Fruchtman S.
    Br J Haematol; 2002 Nov 01; 119(2):558-66. PubMed ID: 12406101
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  • 13. Is fluorescence in situ hybridization a useful method in diagnosis of polycythemia vera patients?
    Zamora L, Espinet B, Florensa L, Besses C, Woessner S, Serrano S, Solé F.
    Cancer Genet Cytogenet; 2004 Jun 01; 151(2):139-45. PubMed ID: 15172751
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  • 14. Trisomy 12 in B-cell chronic lymphocytic leukemia: interphase study by in situ hybridization in 75 patients.
    Coignet L, Berthéas MF, Vasselon C, Jaubert J, Reynaud J, Calmard-Oriol P, Brizard CP, Guyotat D.
    Nouv Rev Fr Hematol (1978); 1993 Apr 01; 35(2):129-34. PubMed ID: 8332448
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  • 15. Gain of 9p in the pathogenesis of polycythemia vera.
    Chen Z, Notohamiprodjo M, Guan XY, Paietta E, Blackwell S, Stout K, Turner A, Richkind K, Trent JM, Lamb A, Sandberg AA.
    Genes Chromosomes Cancer; 1998 Aug 01; 22(4):321-4. PubMed ID: 9669670
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  • 17. 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 01; 32(1 Pt 1):e86-95. PubMed ID: 20089000
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