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571 related items for PubMed ID: 19781438

  • 1. Deletions of chromosome arms 7p and 7q in adult acute myeloid leukemia: a marker chromosome confirmed by array comparative genomic hybridization.
    Woo KS, Kim KE, Kim KH, Kim SH, Park JI, Shaffer LG, Han JY.
    Cancer Genet Cytogenet; 2009 Oct 15; 194(2):71-4. PubMed ID: 19781438
    [Abstract] [Full Text] [Related]

  • 2. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C, Haferlach T, Bursch S, Gerstner D, Schnittger S, Dugas M, Kern W, Löffler H, Hiddemann W.
    Genes Chromosomes Cancer; 2002 Sep 15; 35(1):20-9. PubMed ID: 12203786
    [Abstract] [Full Text] [Related]

  • 3. Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia.
    Brozek I, Babińska M, Kardaś I, Woźniak A, Balcerska A, Hellmann A, Limon J.
    J Appl Genet; 2003 Sep 15; 44(3):401-12. PubMed ID: 12923315
    [Abstract] [Full Text] [Related]

  • 4. [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 15; 20(6):471-6. PubMed ID: 14669212
    [Abstract] [Full Text] [Related]

  • 5. Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
    Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L.
    Genes Chromosomes Cancer; 1999 Mar 15; 24(3):213-21. PubMed ID: 10451701
    [Abstract] [Full Text] [Related]

  • 6. Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies.
    Brezinová J, Zemanová Z, Ransdorfová S, Pavlistová L, Babická L, Housková L, Melichercíková J, Sisková M, Cermák J, Michalová K.
    Cancer Genet Cytogenet; 2007 Feb 15; 173(1):10-6. PubMed ID: 17284364
    [Abstract] [Full Text] [Related]

  • 7. Combined genetic and transcriptional profiling of acute myeloid leukemia with normal and complex karyotypes.
    Lindvall C, Furge K, Björkholm M, Guo X, Haab B, Blennow E, Nordenskjöld M, Teh BT.
    Haematologica; 2004 Sep 15; 89(9):1072-81. PubMed ID: 15377468
    [Abstract] [Full Text] [Related]

  • 8. Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
    Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.
    Cancer Genet Cytogenet; 2006 Feb 15; 165(1):51-63. PubMed ID: 16490597
    [Abstract] [Full Text] [Related]

  • 9. Submicroscopic deletions at 7q region are associated with recurrent chromosome abnormalities in acute leukemia.
    Basiricò R, Pirrotta R, Fabbiano F, Mirto S, Cascio L, Pagano M, Cammarata G, Magrin S, Santoro A.
    Haematologica; 2003 Apr 15; 88(4):429-37. PubMed ID: 12681970
    [Abstract] [Full Text] [Related]

  • 10. AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
    Zatkova A, Merk S, Wendehack M, Bilban M, Muzik EM, Muradyan A, Haferlach C, Haferlach T, Wimmer K, Fonatsch C, Ullmann R.
    Genes Chromosomes Cancer; 2009 Jun 15; 48(6):510-20. PubMed ID: 19306356
    [Abstract] [Full Text] [Related]

  • 11. Genomic Copy Number Variations in the Myelodysplastic Syndrome and Acute Myeloid Leukemia Patients with del(5q) and/or -7/del(7q).
    Zhang R, Kim YM, Wang X, Li Y, Lu X, Sternenberger AR, Li S, Lee JY.
    Int J Med Sci; 2015 Jun 15; 12(9):719-26. PubMed ID: 26392809
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 36(11):1487-95. PubMed ID: 18715689
    [Abstract] [Full Text] [Related]

  • 13. Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML.
    Dawson AJ, Bal S, McTavish B, Tomiuk M, Schroedter I, Ahsanuddin AN, Seftel MD, Vallente R, Mai S, Cotter PD, Hovanes K, Gorre M, Gunn SR.
    Cancer Genet; 2011 Jun 15; 204(6):344-7. PubMed ID: 21763633
    [Abstract] [Full Text] [Related]

  • 14. Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray-based comparative genomic hybridization.
    Tchinda J, Dijkhuizen T, Vlies Pv Pv, Kok K, Horst J.
    Br J Haematol; 2004 Aug 15; 126(4):495-500. PubMed ID: 15287941
    [Abstract] [Full Text] [Related]

  • 15. [Complex additional chromosomal abnormalities of del(5q), del(7q), and +22 in a patient with acute myelomonocytic leukemia carrying inv(16)].
    Nakaya A, Fujita H, Tachibana T, Takemura S, Ishigatsubo Y.
    Rinsho Ketsueki; 2004 Sep 15; 45(9):1061-3. PubMed ID: 15510837
    [Abstract] [Full Text] [Related]

  • 16. Genomic gains and losses influence expression levels of genes located within the affected regions: a study on acute myeloid leukemias with trisomy 8, 11, or 13, monosomy 7, or deletion 5q.
    Schoch C, Kohlmann A, Dugas M, Kern W, Hiddemann W, Schnittger S, Haferlach T.
    Leukemia; 2005 Jul 15; 19(7):1224-8. PubMed ID: 15902281
    [Abstract] [Full Text] [Related]

  • 17. [Analysis of 32 cases of acute leukemia with abnormality of chromosome 7].
    Lu Y, Jin J, Chen ZM, Lou JY, Xu WL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 15; 21(6):596-9. PubMed ID: 15583990
    [Abstract] [Full Text] [Related]

  • 18. Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.
    Evers C, Beier M, Poelitz A, Hildebrandt B, Servan K, Drechsler M, Germing U, Royer HD, Royer-Pokora B.
    Genes Chromosomes Cancer; 2007 Dec 15; 46(12):1119-28. PubMed ID: 17823930
    [Abstract] [Full Text] [Related]

  • 19. Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
    Beyer V, Castagné C, Mühlematter D, Parlier V, Gmür J, Hess U, Kovacsovics T, Meyer-Monard S, Tichelli A, Tobler A, Jacky E, Schanz U, Bargetzi M, Hagemeijer A, de Witte T, van Melle G, Jotterand M.
    Cancer Genet Cytogenet; 2004 Jul 01; 152(1):29-41. PubMed ID: 15193439
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 90(2):194-9. PubMed ID: 15710571
    [Abstract] [Full Text] [Related]

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