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Journal Abstract Search

428 related items for PubMed ID: 15036888

  • 1.
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  • 2. A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.
    Hu J, Shekhter-Levin S, Shaw PH, Bay C, Kochmar S, Surti U.
    Cancer Genet Cytogenet; 2005 Jan 01; 156(1):62-7. PubMed ID: 15588858
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  • 3. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H, Xue Y, Zhang J, Pan J, Dai H, Wu Y, Wang Y, Chen S, Wu D.
    Exp Hematol; 2008 Nov 01; 36(11):1487-95. PubMed ID: 18715689
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  • 6. 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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  • 7. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
    Lunghi M, Casorzo L, De Paoli L, Riccomagno P, Rossi D, Gaidano G.
    Cancer Genet Cytogenet; 2010 Jan 01; 196(1):89-92. PubMed ID: 19963141
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  • 8. Translocation (7;9)(q22;q34) in therapy-related myelodysplastic syndrome after allogeneic bone marrow transplantation for acute myeloblastic leukemia.
    Yamamoto K, Yakushijin K, Kawamori Y, Minagawa K, Katayama Y, Matsui T.
    Cancer Genet Cytogenet; 2007 Jul 01; 176(1):61-6. PubMed ID: 17574966
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  • 9. Therapy-related myelodysplastic syndrome with monosomy 5 after successful treatment of acute myeloid leukemia (M2).
    Ogasawara T, Yasuyama M, Kawauchi K.
    Am J Hematol; 2005 Jun 01; 79(2):136-41. PubMed ID: 15929101
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  • 10. Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia.
    Blau O, Hofmann WK, Baldus CD, Thiel G, Serbent V, Schümann E, Thiel E, Blau IW.
    Exp Hematol; 2007 Feb 01; 35(2):221-9. PubMed ID: 17258071
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  • 11. Pattern of trisomy 1q in hematological malignancies: a single institution experience.
    Djordjević V, Dencić-Fekete M, Jovanović J, Drakulić D, Stevanović M, Janković G, Gotić M.
    Cancer Genet Cytogenet; 2008 Oct 01; 186(1):12-8. PubMed ID: 18786437
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  • 12. Acute myelogenous leukemia with the t(3;12)(q26;p13) translocation: case report and review of the literature.
    Voutsadakis IA, Maillard N.
    Am J Hematol; 2003 Feb 01; 72(2):135-7. PubMed ID: 12555218
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  • 13. Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
    Zhang L, Alsabeh R, Mecucci C, La Starza R, Gorello P, Lee S, Lill M, Schreck R.
    Cancer Genet Cytogenet; 2007 Oct 01; 178(1):42-8. PubMed ID: 17889707
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  • 14. Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells.
    Raynaud SD, Brunet B, Chischportich M, Bayle J, Gratecos N, Pesce A, Dujardin P, Flandrin G, Ayraud N.
    Leukemia; 1994 Feb 01; 8(2):245-9. PubMed ID: 8309249
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  • 15. Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.
    Mehta PA, Harris RE, Davies SM, Kim MO, Mueller R, Lampkin B, Mo J, Myers K, Smolarek TA.
    Cancer Genet Cytogenet; 2010 Dec 01; 203(2):180-6. PubMed ID: 21156231
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  • 16. [Molecular cytogenetic analysis of -7/7q- abnormalities in patients with myeloid malignancies].
    Xiao Y, Liu SH, Liu XP, Qin S, Bo LJ, Li CW, Dai Y, Wang JS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec 01; 20(6):471-6. PubMed ID: 14669212
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  • 17. Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).
    Tosi S, Harbott J, Haas OA, Douglas A, Hughes DM, Ross FM, Biondi A, Scherer SW, Kearney L.
    Leukemia; 1996 Apr 01; 10(4):644-9. PubMed ID: 8618441
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  • 18. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun 01; 78(6):457-67. PubMed ID: 17391336
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  • 19. [der(1;7) (q10;p10) in three patients with malignant hematologic disorders].
    Yokoo H, Okada Y, Tominaga K, Tsuji M, Takagi T, Maseki N, Sakurai M, Kaneko Y.
    Rinsho Ketsueki; 1992 Dec 01; 33(12):1829-33. PubMed ID: 1479694
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  • 20. Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia.
    Park TS, Cheong JW, Song J, Choi JR.
    Leuk Res; 2009 Jul 01; 33(7):1001-4. PubMed ID: 19155067
    [Abstract] [Full Text] [Related]

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