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508 related items for PubMed ID: 17509681

  • 1. dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
    Alfaro R, Pérez-Granero A, Durán MA, Besalduch J, Rosell J, Bernués M.
    Leuk Res; 2008 Jan; 32(1):159-61. PubMed ID: 17509681
    [Abstract] [Full Text] [Related]

  • 2. Inverted duplication dup(1)(q32q21) as sole aberration in lymphoid and myeloid malignancies.
    Bacher U, Schnittger S, Grüneisen A, Haferlach T, Kern W, Haferlach C.
    Cancer Genet Cytogenet; 2009 Jan 15; 188(2):108-11. PubMed ID: 19100515
    [Abstract] [Full Text] [Related]

  • 3. Duplication of chromosome 1 [dup(1)(q21q32)] as the sole cytogenetic abnormality in a patient previously treated for AML.
    Beach DF, Barnoski BL, Aviv H, Patel V, Schwarting R, Strair R, Lachant NA.
    Cancer Genet; 2012 Dec 15; 205(12):665-8. PubMed ID: 23168243
    [Abstract] [Full Text] [Related]

  • 4. Duplications of the long arm of both chromosome 1, dup(1)(q21q32), leading to tetrasomy 1q in myelodysplastic syndrome.
    Kim JE, Woo KS, Kim KE, Kim SH, Park JI, Shaffer LG, Han JY.
    Leuk Res; 2010 Aug 15; 34(8):e210-2. PubMed ID: 20299094
    [No Abstract] [Full Text] [Related]

  • 5. Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY.
    Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskova J, Heck B, Tone LG.
    Leuk Res; 2005 Dec 15; 29(12):1465-7. PubMed ID: 15964069
    [Abstract] [Full Text] [Related]

  • 6. Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
    Millington K, Hudnall SD, Northup J, Panova N, Velagaleti G.
    Exp Mol Pathol; 2008 Apr 15; 84(2):189-93. PubMed ID: 18339374
    [Abstract] [Full Text] [Related]

  • 7. Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
    Park TS, Song J, Lee JH, Kim JS, Yang WI, Choi JR.
    Ann Clin Lab Sci; 2009 Apr 15; 39(2):176-81. PubMed ID: 19429805
    [Abstract] [Full Text] [Related]

  • 8. Consecutive chromosomal studies in patients with myelodysplastic syndrome (MDS). Czechoslovak MDS Cooperative Group.
    Michalova K, Musilova J, Zemanova Z.
    Ann Genet; 1991 Apr 15; 34(3-4):212-8. PubMed ID: 1809229
    [Abstract] [Full Text] [Related]

  • 9. Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11.
    Caligiuri MA, Strout MP, Schichman SA, Mrózek K, Arthur DC, Herzig GP, Baer MR, Schiffer CA, Heinonen K, Knuutila S, Nousiainen T, Ruutu T, Block AW, Schulman P, Pedersen-Bjergaard J, Croce CM, Bloomfield CD.
    Cancer Res; 1996 Mar 15; 56(6):1418-25. PubMed ID: 8640834
    [Abstract] [Full Text] [Related]

  • 10. Cytogenetic analysis in patients with myelodysplastic syndrome.
    Hu N, Bian M.
    Proc Chin Acad Med Sci Peking Union Med Coll; 1990 Mar 15; 5(3):135-9. PubMed ID: 2098765
    [Abstract] [Full Text] [Related]

  • 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 15; 186(1):12-8. PubMed ID: 18786437
    [Abstract] [Full Text] [Related]

  • 12. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome.
    Kakazu N, Taniwaki M, Horiike S, Nishida K, Tatekawa T, Nagai M, Takahashi T, Akaogi T, Inazawa J, Ohki M, Abe T.
    Genes Chromosomes Cancer; 1999 Dec 15; 26(4):336-45. PubMed ID: 10534769
    [Abstract] [Full Text] [Related]

  • 13. [Clinical and experimental study of 38 cases with trisomy 8].
    Xu WL, Jin J, Chen ZM, Lou JY, Yu YB.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec 15; 20(6):528-31. PubMed ID: 14669224
    [Abstract] [Full Text] [Related]

  • 14. A der(14)t(1;14)(q12;p11) in chronic myelomonocytic leukemia.
    Djordjevic V, Jankovic G, Suvajdzic N, Marisavljevic D, Pantic M, Bogdanovic A, Sefer D, Dencic M, Colovic M.
    Cancer Genet Cytogenet; 2005 Jul 01; 160(1):89-93. PubMed ID: 15949578
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes.
    Paulsson K, Johansson B.
    Pathol Biol (Paris); 2007 Feb 01; 55(1):37-48. PubMed ID: 16697122
    [Abstract] [Full Text] [Related]

  • 17. Gain of 1q in pediatric myelodysplastic syndromes.
    Morerio C, Rapella A, Tassano E, Lanino E, Micalizzi C, Rosanda C, Panarello C.
    Leuk Res; 2006 Nov 01; 30(11):1437-41. PubMed ID: 16472857
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 20(5):840-6. PubMed ID: 16498392
    [Abstract] [Full Text] [Related]

  • 19. Myelodysplastic syndrome associated with trisomy 2.
    Heller M, Provan D, Amess JA, Dixon-McIver A.
    Clin Lab Haematol; 2005 Aug 01; 27(4):270-3. PubMed ID: 16048496
    [Abstract] [Full Text] [Related]

  • 20. Constitutional t(5;7)(q11;p15) rearranged to acquire monosomy 7q and trisomy 1q in a patient with myelodysplastic syndrome transforming to acute myelocytic leukemia.
    Ganly P, McDonald M, Spearing R, Morris CM.
    Cancer Genet Cytogenet; 2004 Mar 01; 149(2):125-30. PubMed ID: 15036888
    [Abstract] [Full Text] [Related]

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