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Journal Abstract Search

256 related items for PubMed ID: 20633770

  • 1. A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome.
    Lizcova L, Zemanova Z, Malinova E, Jarosova M, Mejstrikova E, Smisek P, Pospisilova D, Stary J, Michalova K.
    Cancer Genet Cytogenet; 2010 Aug; 201(1):52-6. PubMed ID: 20633770
    [Abstract] [Full Text] [Related]

  • 2. 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; 5(2):55-9. PubMed ID: 16096854
    [Abstract] [Full Text] [Related]

  • 3. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
    Maserati E, Pressato B, Valli R, Minelli A, Sainati L, Patitucci F, Marletta C, Mastronuzzi A, Poli F, Lo Curto F, Locatelli F, Danesino C, Pasquali F.
    Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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; 155(1):67-73. PubMed ID: 15527905
    [Abstract] [Full Text] [Related]

  • 6. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
    Praulich I, Tauscher M, Göhring G, Glaser S, Hofmann W, Feurstein S, Flotho C, Lichter P, Niemeyer CM, Schlegelberger B, Steinemann D.
    Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
    [Abstract] [Full Text] [Related]

  • 7. [Chromosomal aberrations in myelodysplastic syndrome].
    Ol'shanskaia IuV, Domracheva EV, Udovichenko AI, Vodinskaia LA, Zakharova AV, Parovichnikova EN, Tsvetaeva NV, Mikhaĭlova EA, Glasko EN, Kolosova LIu, Kokhno AN, Tikhonova LIu, Shitareva TV, Smirnova EA, Alimova GA, Shirin AD, Vinogradova OIu, Khoroshko ND, Savchenko VG.
    Ter Arkh; 2005 Oct; 77(7):27-33. PubMed ID: 16116905
    [Abstract] [Full Text] [Related]

  • 8. Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
    Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, De Braekeleer M.
    Eur J Haematol; 2007 Jun; 78(6):457-67. PubMed ID: 17391336
    [Abstract] [Full Text] [Related]

  • 9. [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; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

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  • 12. [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]

  • 13. [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]

  • 14. 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; 93(7):1001-8. PubMed ID: 18591625
    [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; 35(2):221-9. PubMed ID: 17258071
    [Abstract] [Full Text] [Related]

  • 16. Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
    Maserati E, Minelli A, Pressato B, Valli R, Crescenzi B, Stefanelli M, Menna G, Sainati L, Poli F, Panarello C, Zecca M, Curto FL, Mecucci C, Danesino C, Pasquali F.
    Genes Chromosomes Cancer; 2006 Apr; 45(4):375-82. PubMed ID: 16382447
    [Abstract] [Full Text] [Related]

  • 17. [A novel translocation t(1;18)(p31;p11) in a patient with myelodysplastic syndrome].
    Du B, Wu YF, Pan JL, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):74-5. PubMed ID: 15696486
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Conventional cytogenetics and fluorescence in situ hybridization in persistent cytopenias and myelodysplastic syndromes in childhood.
    Touliatou V, Kolialexi A, Tsangaris GT, Moschovi M, Polychronopoulou S, Mavrou A.
    Anticancer Res; 2004 Feb; 24(6):3945-9. PubMed ID: 15736436
    [Abstract] [Full Text] [Related]

  • 20. Isochromosome of a deleted 20q: a rare but recurrent chromosome abnormality in myelodysplastic syndromes.
    Saunders K, Czepulkowski B, Sivalingam R, Hayes JP, Aldouri M, Sekhar M, Cummins M, Ho A, Mufti GJ.
    Cancer Genet Cytogenet; 2005 Jan 15; 156(2):154-7. PubMed ID: 15642396
    [Abstract] [Full Text] [Related]

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