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1285 related items for PubMed ID: 8618444

  • 1. Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology.
    Bernell P, Jacobsson B, Nordgren A, Hast R.
    Leukemia; 1996 Apr; 10(4):662-8. PubMed ID: 8618444
    [Abstract] [Full Text] [Related]

  • 2. Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH).
    Han K, Lee W, Harris CP, Kim W, Shim S, Meisner LF.
    Leukemia; 1994 Jan; 8(1):81-6. PubMed ID: 8289503
    [Abstract] [Full Text] [Related]

  • 3. Detection of monosomy 7 and trisomies 8 and 11 in myelodysplastic disorders by interphase fluorescent in situ hybridization. Comparison with acute non-lymphocytic leukemias.
    Brizard F, Brizard A, Guilhot F, Tanzer J, Berger R.
    Leukemia; 1994 Jun; 8(6):1005-11. PubMed ID: 8207973
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  • 5. Cytogenetic clonality analysis in myelodysplastic syndrome: monosomy 7 can be demonstrated in the myeloid and in the lymphoid lineage.
    van Lom K, Hagemeijer A, Smit E, Hählen K, Groeneveld K, Löwenberg B.
    Leukemia; 1995 Nov; 9(11):1818-21. PubMed ID: 7475268
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  • 7. Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes.
    Flactif M, Lai JL, Preudhomme C, Fenaux P.
    Leukemia; 1994 Jun; 8(6):1012-8. PubMed ID: 8207974
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  • 8. Fluorescence in situ hybridization (FISH) detection of trisomy 8 in myeloid cells in chronic myeloid leukemia (CML): a study of archival blood and bone marrow smears.
    Nguyen PL, Arthur DC, Litz CE, Brunning RD.
    Leukemia; 1994 Oct; 8(10):1654-62. PubMed ID: 7934161
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  • 9. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations.
    Lai JL, Preudhomme C, Zandecki M, Flactif M, Vanrumbeke M, Lepelley P, Wattel E, Fenaux P.
    Leukemia; 1995 Mar; 9(3):370-81. PubMed ID: 7885035
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  • 10. Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders.
    Baurmann H, Cherif D, Berger R.
    Leukemia; 1993 Mar; 7(3):384-91. PubMed ID: 8445944
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  • 12. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P, Balogh E, Jakab Z, Germán P, Bodnár F, Kiss A, Telek B, Oláh E.
    Orv Hetil; 2002 Dec 15; 143(50):2775-9. PubMed ID: 12583317
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 29(4):299-303. PubMed ID: 18199987
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  • 14. Differences in cell lineage involvement between MDS-AML and de novo AML studied by fluorescence in situ hybridization in combination with morphology.
    Bernell P, Arvidsson I, Hast R, Jacobsson B, Stenke L.
    Eur J Haematol; 1997 Apr 15; 58(4):241-5. PubMed ID: 9186534
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  • 15. Neutrophil dysplasia is not a specific feature of the abnormal chromosomal clone in myelodysplastic syndromes.
    Hast R, Eriksson M, Widell S, Arvidsson I, Bemell P.
    Leuk Res; 1999 Jun 15; 23(6):579-84. PubMed ID: 10374851
    [Abstract] [Full Text] [Related]

  • 16. Detection of monosomy 7 by fluorescence in situ hybridization in acute nonlymphocytic leukemia and myelodysplastic syndrome.
    Nakagawa H.
    Jpn J Hum Genet; 1993 Sep 15; 38(3):257-66. PubMed ID: 8260718
    [Abstract] [Full Text] [Related]

  • 17. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
    Paulsson K, Heidenblad M, Strömbeck B, Staaf J, Jönsson G, Borg A, Fioretos T, Johansson B.
    Leukemia; 2006 May 15; 20(5):840-6. PubMed ID: 16498392
    [Abstract] [Full Text] [Related]

  • 18. Physician Education: Myelodysplastic Syndrome.
    Yoshida Y.
    Oncologist; 1996 May 15; 1(4):284-287. PubMed ID: 10388004
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  • 19. Detection of trisomy 8 by fluorescence in situ hybridization on bone marrow smears from patients with subtle myelodysplastic changes.
    Brynes RK, Swayne D, McCourty A, Dosik GM, Traweek ST, Slovak ML.
    Arch Pathol Lab Med; 1994 Dec 15; 118(12):1196-200. PubMed ID: 7979913
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  • 20. 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 15; 35(2):221-9. PubMed ID: 17258071
    [Abstract] [Full Text] [Related]

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