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136 related items for PubMed ID: 15066323

  • 1. Chromosomal insertion involving MLL in childhood acute myeloblastic leukemia (M4).
    Lafay-Cousin L, Soenen V, Mazingue F, Preudhomme C, Laï JL, Andrieux J.
    Cancer Genet Cytogenet; 2004 Apr 15; 150(2):153-5. PubMed ID: 15066323
    [Abstract] [Full Text] [Related]

  • 2. [Rearrangements of the mixed lineage leukemia gene in acute myeloid leukemia].
    Zhang LJ, Lu XL, He J, Li Y.
    Zhonghua Yi Xue Za Zhi; 2006 Aug 29; 86(32):2256-60. PubMed ID: 17064570
    [Abstract] [Full Text] [Related]

  • 3. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P, Harrison CJ, Jarosová M, Foroni L.
    Haematologica; 2005 May 29; 90(5):602-11. PubMed ID: 15921375
    [Abstract] [Full Text] [Related]

  • 4. A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia.
    de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, de Figueiredo AF, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML.
    Cancer Genet Cytogenet; 2009 Feb 29; 189(1):59-62. PubMed ID: 19167614
    [Abstract] [Full Text] [Related]

  • 5. [MLL rearrangements in acute leukemias].
    Urioste M, Arranz E, Martínez-Delgado B, Soto C, Román A, Pérez I, Mayayo M, Pérez-Pons C, Barroso A, Benítez J.
    Sangre (Barc); 1999 Dec 29; 44(6):464-8. PubMed ID: 10822761
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  • 6. X chromosome insertion in the MLL gene in a case of childhood acute myeloblastic leukemia.
    Arnaud B, Morel F, Douet-Guilbert N, Le Bris MJ, De Braekeleer M.
    Cancer Genet Cytogenet; 2004 Jul 15; 152(2):149-52. PubMed ID: 15262436
    [Abstract] [Full Text] [Related]

  • 7. Detection of inv(16) and t(16;16) by fluorescence in situ hybridization in acute myeloid leukemia M4Eo.
    Hernández JM, González MB, Granada I, Gutiérrez N, Chillón C, Ramos F, Ribera JM, González M, Feliu E, San Miguel J.
    Haematologica; 2000 May 15; 85(5):481-5. PubMed ID: 10800163
    [Abstract] [Full Text] [Related]

  • 8. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype.
    Yamamoto K, Hato A, Minagawa K, Yakushijin K, Urahama N, Gomyo H, Sada A, Okamura A, Ito M, Matsui T.
    Cancer Genet Cytogenet; 2004 Nov 15; 155(1):67-73. PubMed ID: 15527905
    [Abstract] [Full Text] [Related]

  • 9. Overlapping deletion regions at 11q23 in myelodysplastic syndrome and chronic lymphocytic leukemia, characterized by a novel BAC probe set.
    Siew-Gek Lee A, Rudduck-Sivaswaren C, Khun-Hong Lie D, Li-Ming Chua C, Tien SL, Morsberger L, Griffin CA.
    Cancer Genet Cytogenet; 2004 Sep 15; 153(2):151-7. PubMed ID: 15350305
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Translocation (10;11)(p12;q23) in childhood acute myeloid leukemia: incidence and complex mechanism.
    Stasevich I, Utskevich R, Kustanovich A, Litvinko N, Savitskaya T, Chernyavskaya S, Saharova O, Aleinikova O.
    Cancer Genet Cytogenet; 2006 Sep 01; 169(2):114-20. PubMed ID: 16938568
    [Abstract] [Full Text] [Related]

  • 12. Molecular cytogenetic characterization of rearrangements involving 12p in leukemia.
    Vieira L, Marques B, Cavaleiro C, Ambrósio AP, Jorge M, Neto A, Costa JM, Júnior EC, Boavida MG.
    Cancer Genet Cytogenet; 2005 Mar 01; 157(2):134-9. PubMed ID: 15721634
    [Abstract] [Full Text] [Related]

  • 13. A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.
    Tirado CA, Lager J, Rosoff PM, Golembiski-Ruiz V, Gong JZ, Goodman BK.
    Cancer Genet Cytogenet; 2004 Oct 01; 154(1):57-9. PubMed ID: 15381373
    [Abstract] [Full Text] [Related]

  • 14. Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
    Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T.
    Cancer Genet Cytogenet; 2008 Apr 01; 182(1):56-60. PubMed ID: 18328953
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  • 16. Cohabiting t(12;22) and inv(3) primary rearrangements in an acute myelomonocytic leukemia (FAB M4) cell line.
    MacLeod RA, Hu ZB, Kaufmann M, Drexler HG.
    Genes Chromosomes Cancer; 1996 Jun 01; 16(2):144-8. PubMed ID: 8818662
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  • 19. Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia.
    Stasik C, Ganguly S, Cunningham MT, Hagemeister S, Persons DL.
    Cancer Genet Cytogenet; 2006 Jul 15; 168(2):146-9. PubMed ID: 16843104
    [Abstract] [Full Text] [Related]

  • 20. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y, Xu W, Liu Q, Pan J, Qiu H, Wang R, Qiao C, Jiang Y, Zhang S, Fan L, Zhang J, Shen Y, Xue Y, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 15; 25(5):579-82. PubMed ID: 18841577
    [Abstract] [Full Text] [Related]

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