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PUBMED FOR HANDHELDS

Journal Abstract Search


541 related items for PubMed ID: 19963141

  • 21.
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  • 22. [Multiplex fluorescence in situ hybridization in detecting complex chromosomal aberrations in myelodysplastic syndromes].
    Xiao B, Li JY, Pan JL, Ma L, Qiu HR, Wu YF, Xue YQ.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Sep; 26(9):513-6. PubMed ID: 16468325
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  • 23. Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
    Millington K, Hudnall SD, Northup J, Panova N, Velagaleti G.
    Exp Mol Pathol; 2008 Apr; 84(2):189-93. PubMed ID: 18339374
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  • 26. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
    Park TS, Song J, Lee JH, Kim JS, Yang WI, Choi JR.
    Ann Clin Lab Sci; 2009 Apr; 39(2):176-81. PubMed ID: 19429805
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  • 27. der(3)t(3;5). Another recurring abnormality in myelodysplastic disorder.
    Lindgren V, Gibson L, Yang-Feng TL.
    Cancer Genet Cytogenet; 1991 Jul 01; 54(1):129-31. PubMed ID: 2065307
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  • 29. Clinical, cytogenetic and dual-color FISH studies on five cases of myelodysplastic syndrome or acute myeloid leukemia patients with 1;7 translocation.
    Shen Y, Xue Y, Li J, Pan J, Wu Y.
    Chin Med J (Engl); 2003 Feb 01; 116(2):231-4. PubMed ID: 12775237
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  • 31. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Feb 01; 16(3):257-68. PubMed ID: 16259323
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  • 38. Myelodysplastic syndrome associated with trisomy 2.
    Heller M, Provan D, Amess JA, Dixon-McIver A.
    Clin Lab Haematol; 2005 Aug 01; 27(4):270-3. PubMed ID: 16048496
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