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340 related items for PubMed ID: 11484160

  • 1. [Detection of monosomy 7 or 7q- in cases of myelodysplastic syndrome].
    Shen Y, Xue Y, Li J, Guo Y, Pan J, Wu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Aug; 18(4):255-8. PubMed ID: 11484160
    [Abstract] [Full Text] [Related]

  • 2. 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; 29(4):299-303. PubMed ID: 18199987
    [Abstract] [Full Text] [Related]

  • 3. [Detection of -5/5q- chromosome abnormality in myelodysplastic syndromes by interphase fluorescence in situ hybridization].
    Shen Y, Xue Y, Li J.
    Zhonghua Xue Ye Xue Za Zhi; 2001 Oct; 22(10):517-9. PubMed ID: 11769675
    [Abstract] [Full Text] [Related]

  • 4. [Detection of trisomy 8 with interphase fluorescence in situ hybridization in myelodysplastic syndromes].
    Li J, Pan J, Xue Y, Wu C, Xie X, Guo Y, Ruan C.
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):179-81. PubMed ID: 11876976
    [Abstract] [Full Text] [Related]

  • 5. [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; 20(6):471-6. PubMed ID: 14669212
    [Abstract] [Full Text] [Related]

  • 6. [Detection of common chromosome abnormalities in myelodysplastic syndrome with a panel fluorescence in situ hybridization].
    Shen Y, Xue Y, Li J, Pan J, Wu Y, Chen S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):160-3. PubMed ID: 12673589
    [Abstract] [Full Text] [Related]

  • 7. Fluorescence in situ hybridization testing for -5/5q, -7/7q, +8, and del(20q) in primary myelodysplastic syndrome correlates with conventional cytogenetics in the setting of an adequate study.
    Pitchford CW, Hettinga AC, Reichard KK.
    Am J Clin Pathol; 2010 Feb; 133(2):260-4. PubMed ID: 20093235
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?
    Ademà V, Hernández JM, Abáigar M, Lumbreras E, Such E, Calull A, Dominguez E, Arenillas L, Mallo M, Cervera J, Marugán I, Tormo M, García F, González T, Luño E, Sanzo C, Martín ML, Fernández M, Costa D, Blázquez B, Barreña B, Marco F, Batlle A, Buño I, Martínez-Laperche C, Noriega V, Collado R, Ivars D, Carbonell F, Vallcorba I, Melero J, Delgado E, Vargas MT, Grau J, Salido M, Espinet B, Melero C, Florensa L, Pedro C, Solé F.
    Leuk Res; 2013 Apr 01; 37(4):416-21. PubMed ID: 23337401
    [Abstract] [Full Text] [Related]

  • 10. [Detection of cytogenetic abnormalities involving chromosomes 5,7 and 8 in myelodysplastic syndromes with fluorescence in situ hybridization and its clinical significance].
    Cai Y, Qin YW, Wang C, Yang J, Yan SK.
    Zhonghua Xue Ye Xue Za Zhi; 2007 Jan 01; 28(1):6-10. PubMed ID: 17649717
    [Abstract] [Full Text] [Related]

  • 11. Detection of monosomy 7 by fluorescence in situ hybridization in acute nonlymphocytic leukemia and myelodysplastic syndrome.
    Nakagawa H.
    Jpn J Hum Genet; 1993 Sep 01; 38(3):257-66. PubMed ID: 8260718
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 8(6):1005-11. PubMed ID: 8207973
    [Abstract] [Full Text] [Related]

  • 13. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ, Li JY, Xiao B, Zhu Y, Liu Q, Pan JL, Qiu HR, Fan L, Zhang SJ, Lu RN, Xu W, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec 01; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

  • 14. [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]

  • 15. Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes.
    Flactif M, Lai JL, Preudhomme C, Fenaux P.
    Leukemia; 1994 Jun 15; 8(6):1012-8. PubMed ID: 8207974
    [Abstract] [Full Text] [Related]

  • 16. Interphase cytogenetics of hematological cancer: comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome specific DNA probes.
    Poddighe PJ, Moesker O, Smeets D, Awwad BH, Ramaekers FC, Hopman AH.
    Cancer Res; 1991 Apr 01; 51(7):1959-67. PubMed ID: 2004382
    [Abstract] [Full Text] [Related]

  • 17. Conventional and molecular cytogenetic findings of myelodysplastic syndrome patients.
    Yilmaz Z, Sahin FI, Kizilkilic E, Karakus S, Boga C, Ozdogu H.
    Clin Exp Med; 2005 Jul 01; 5(2):55-9. PubMed ID: 16096854
    [Abstract] [Full Text] [Related]

  • 18. Acquisition of a Ph chromosome with minor BCR/ABL fusion in treatment-related myelodysplastic syndrome with chromosome 7 abnormalities in a patient treated for Hodgkin disease.
    Kneller A, Cohen N, Berkowicz M, Reichart M, Rosner E, Sokolovski M, Nagler A, Rechavi G, Amariglio N, Trakhtenbrot L.
    Cancer Genet Cytogenet; 2005 May 01; 159(1):58-62. PubMed ID: 15860359
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 173(1):10-6. PubMed ID: 17284364
    [Abstract] [Full Text] [Related]

  • 20. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
    Mallo M, Arenillas L, Espinet B, Salido M, Hernández JM, Lumbreras E, del Rey M, Arranz E, Ramiro S, Font P, González O, Renedo M, Cervera J, Such E, Sanz GF, Luño E, Sanzo C, González M, Calasanz MJ, Mayans J, García-Ballesteros C, Amigo V, Collado R, Oliver I, Carbonell F, Bureo E, Insunza A, Yañez L, Muruzabal MJ, Gómez-Beltrán E, Andreu R, León P, Gómez V, Sanz A, Casasola N, Moreno E, Alegre A, Martín ML, Pedro C, Serrano S, Florensa L, Solé F.
    Haematologica; 2008 Jul 01; 93(7):1001-8. PubMed ID: 18591625
    [Abstract] [Full Text] [Related]

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