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Journal Abstract Search

88 related items for PubMed ID: 20306244

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  • 2. 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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  • 7. [Importance of cytogenetics in the study of acute non-lymphoblastic leukemias].
    Prieto F, Badía L, Palau F, Beneyto M, Montero MR, Martínez-Castellano F.
    Sangre (Barc); 1991 Jun; 36(3):229-35. PubMed ID: 1948543
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  • 8. A patient with de novo AML M1 and t(16;21) with karyotype evolution.
    Zatkova A, Fonatsch C, Sperr WR, Valent P.
    Leuk Res; 2007 Sep; 31(9):1319-21. PubMed ID: 17126398
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  • 10. A cryptic three-way translocation involving chromosomes 8, 14, and 21 in a case of acute myeloid leukemia subtype M1.
    Lau LC, Koh LP, Lim TH, Loo LE, Tien SL.
    Cancer Genet Cytogenet; 2005 Nov; 163(1):86-90. PubMed ID: 16271963
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  • 12. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
    Fröhling S, Kayser S, Mayer C, Miller S, Wieland C, Skelin S, Schlenk RF, Döhner H, Döhner K, AML Study Group Ulm.
    Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
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  • 13. Clinical significance of the most common chromosome translocations in adult acute myeloid leukemia.
    Mrózek K, Bloomfield CD.
    J Natl Cancer Inst Monogr; 2008 Feb; (39):52-7. PubMed ID: 18648004
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  • 14. Prognostic impact of specific chromosomal aberrations in a large group of pediatric patients with acute myeloid leukemia treated uniformly according to trial AML-BFM 98.
    von Neuhoff C, Reinhardt D, Sander A, Zimmermann M, Bradtke J, Betts DR, Zemanova Z, Stary J, Bourquin JP, Haas OA, Dworzak MN, Creutzig U.
    J Clin Oncol; 2010 Jun 01; 28(16):2682-9. PubMed ID: 20439630
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  • 19. Three-way complex translocations in infant acute myeloid leukemia with t(7;12)(q36;p13): the incidence and correlation of a HLXB9 overexpression.
    Park J, Kim M, Lim J, Kim Y, Han K, Lee J, Chung NG, Cho B, Kim HK.
    Cancer Genet Cytogenet; 2009 Jun 01; 191(2):102-5. PubMed ID: 19446746
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