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266 related items for PubMed ID: 17556074

  • 1. Incidence of submicroscopic deletions vary according to disease entities and chromosomal translocations in hematologic malignancies: investigation by fluorescence in situ hybridization.
    Moon HW, Chang YH, Kim TY, Oh BR, Min HC, Kim BK, Ahn HS, Cho HI, Lee DS.
    Cancer Genet Cytogenet; 2007 Jun; 175(2):166-8. PubMed ID: 17556074
    [Abstract] [Full Text] [Related]

  • 2. The role of fluorescence in situ hybridization (FISH) for monitoring hematologic malignancies with BCR/ABL or ETO/AML1 rearrangement: a comparative study with FISH and G-banding on 919 consecutive specimens of hematologic malignancies.
    Lee DY, Cho HI, Kang YH, Yun SS, Park SY, Lee YS, Kim Y, Lee DS.
    Cancer Genet Cytogenet; 2004 Jul 01; 152(1):1-7. PubMed ID: 15193435
    [Abstract] [Full Text] [Related]

  • 3. The incidence of submicroscopic deletions in reciprocal translocations is similar in acute myeloid leukemia, BCR-ABL positive acute lymphoblastic leukemia, and chronic myeloid leukemia.
    Bacher U, Schnittger S, Kern W, Hiddemann W, Haferlach T, Schoch C.
    Haematologica; 2005 Apr 01; 90(4):558-9. PubMed ID: 15820957
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  • 6. 3'CBFbeta deletion associated with inv(16) in acute myeloid leukemia.
    Kelly J, Foot NJ, Conneally E, Enright H, Humphreys M, Saunders K, Neat MJ.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):122-6. PubMed ID: 16213359
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  • 7. The presence of TEL/AML1 rearrangement and cryptic deletion of the TEL gene in adult acute lymphoblastic leukemia (ALL).
    Lee DS, Kim YR, Cho HK, Lee CK, Lee JH, Cho HI.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):176-8. PubMed ID: 16213368
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  • 8. Co-existence of multiple subclones in TEL-AML1 at diagnosis of acute lymphoblastic leukaemia in association with submicroscopic deletion of AML1.
    Rothman R, Trakhtenbrot L, Bielorai B, Izraeli S, Ishoev G, Amariglio N, Rechavi G, Toren A.
    Br J Haematol; 2005 May 15; 129(4):491-8. PubMed ID: 15877731
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  • 9. Molecular cytogenetic and clinical findings in ETV6/ABL1-positive leukemia.
    Van Limbergen H, Beverloo HB, van Drunen E, Janssens A, Hählen K, Poppe B, Van Roy N, Marynen P, De Paepe A, Slater R, Speleman F.
    Genes Chromosomes Cancer; 2001 Mar 15; 30(3):274-82. PubMed ID: 11170285
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  • 10. Identification of additional cytogenetic and molecular genetic abnormalities in acute myeloid leukaemia with t(8;21)/AML1-ETO.
    Kuchenbauer F, Schnittger S, Look T, Gilliland G, Tenen D, Haferlach T, Hiddemann W, Buske C, Schoch C.
    Br J Haematol; 2006 Sep 15; 134(6):616-9. PubMed ID: 16938118
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  • 11. Chromatin structural elements and chromosomal translocations in leukemia.
    Zhang Y, Rowley JD.
    DNA Repair (Amst); 2006 Sep 08; 5(9-10):1282-97. PubMed ID: 16893685
    [Abstract] [Full Text] [Related]

  • 12. [Clinical utility of fluorescence in-situ hybridization profile test in detecting genetic aberrations in acute leukemia].
    Kim SR, Kim HJ, Kim SH.
    Korean J Lab Med; 2009 Oct 08; 29(5):371-8. PubMed ID: 19893343
    [Abstract] [Full Text] [Related]

  • 13. Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
    Ahmad F, Kokate P, Chheda P, Dalvi R, Das BR, Mandava S.
    Cancer Genet Cytogenet; 2008 Jan 15; 180(2):153-7. PubMed ID: 18206543
    [Abstract] [Full Text] [Related]

  • 14. Molecular cytogenetic analysis of gene rearrangements in childhood acute lymphoblastic leukemia.
    Woo HY, Kim DW, Park H, Seong KW, Koo HH, Kim SH.
    J Korean Med Sci; 2005 Feb 15; 20(1):36-41. PubMed ID: 15716599
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  • 15. Cryptic and partial deletions of PRDM16 and RUNX1 without t(1;21)(p36;q22) and/or RUNX1-PRDM16 fusion in a case of progressive chronic myeloid leukemia: a complex chromosomal rearrangement of underestimated frequency in disease progression?
    Deluche L, Joha S, Corm S, Daudignon A, Geffroy S, Quief S, Villenet C, Kerckaert JP, Laï JL, Preudhomme C, Roche-Lestienne C.
    Genes Chromosomes Cancer; 2008 Dec 15; 47(12):1110-7. PubMed ID: 18767145
    [Abstract] [Full Text] [Related]

  • 16. Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization.
    Nebral K, König M, Schmidt HH, Lutz D, Sperr WR, Kalwak K, Brugger S, Dworzak MN, Haas OA, Strehl S.
    Haematologica; 2005 Jun 15; 90(6):746-52. PubMed ID: 15951287
    [Abstract] [Full Text] [Related]

  • 17. Interphase FISH on TEL/AML1 positive acute lymphoblastic leukemia relapses--analysis of clinical relevance of additional TEL and AML1 copy number changes.
    Peter A, Heiden T, Taube T, Körner G, Seeger K.
    Eur J Haematol; 2009 Nov 15; 83(5):420-32. PubMed ID: 19594616
    [Abstract] [Full Text] [Related]

  • 18. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis.
    Kolomietz E, Al-Maghrabi J, Brennan S, Karaskova J, Minkin S, Lipton J, Squire JA.
    Blood; 2001 Jun 01; 97(11):3581-8. PubMed ID: 11369654
    [Abstract] [Full Text] [Related]

  • 19. Prognostic significance of del(20q) in patients with hematological malignancies.
    Brezinová J, Zemanová Z, Ransdorfová S, Sindelárová L, Sisková M, Neuwirtová R, Cermák J, Michalová K.
    Cancer Genet Cytogenet; 2005 Jul 15; 160(2):188-92. PubMed ID: 15993278
    [Abstract] [Full Text] [Related]

  • 20. [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]

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