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Journal Abstract Search

159 related items for PubMed ID: 12228913

  • 21. Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique.
    Karaoguz MY, Nas T, Konaç E, Ince D, Pala E, Menevse S.
    J Obstet Gynaecol Res; 2005 Dec; 31(6):508-13. PubMed ID: 16343250
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Molecular cytogenetic aberrations in 21 Chinese patients with plasma cell leukemia.
    Xu W, Li JY, Fan L, Chen LJ, Qiu HR, Qiu HX, Lu H.
    Int J Lab Hematol; 2009 Jun; 31(3):338-43. PubMed ID: 18284415
    [Abstract] [Full Text] [Related]

  • 24. [Clinical and experimental retrospective analysis on acute leukemia with trisomy 4 cell].
    Pan JL, Xue YQ, Qiu HY, Zhang J, Wu YF, Wang Y, Shen J, Zhu YJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):369-72. PubMed ID: 17680522
    [Abstract] [Full Text] [Related]

  • 25. Trisomy 4 as the sole cytogenetic abnormality in a patient with T-cell acute lymphoblastic leukemia.
    Gupta V, Chun K.
    Cancer Genet Cytogenet; 2004 Jul 15; 152(2):158-62. PubMed ID: 15262438
    [Abstract] [Full Text] [Related]

  • 26. 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 15; 90(2):194-9. PubMed ID: 15710571
    [Abstract] [Full Text] [Related]

  • 27. Frequent increase of DNA copy number in the 2q24 chromosomal region and its association with a poor clinical outcome in hepatoblastoma: cytogenetic and comparative genomic hybridization analysis.
    Kumon K, Kobayashi H, Namiki T, Tsunematsu Y, Miyauchi J, Kikuta A, Horikoshi Y, Komada Y, Hatae Y, Eguchi H, Kaneko Y.
    Jpn J Cancer Res; 2001 Aug 15; 92(8):854-62. PubMed ID: 11509117
    [Abstract] [Full Text] [Related]

  • 28. Detection of chromosomal abnormalities associated with chronic lymphocytic leukemia: what is the best method?
    El-Taweel M, Barin C, Cymbalista F, Eclache V.
    Cancer Genet Cytogenet; 2009 Nov 15; 195(1):37-42. PubMed ID: 19837267
    [Abstract] [Full Text] [Related]

  • 29. Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
    Starke H, Mrasek K, Liehr T.
    J Histochem Cytochem; 2005 Mar 15; 53(3):359-60. PubMed ID: 15750019
    [Abstract] [Full Text] [Related]

  • 30. A comprehensive karyotypic study on human hepatocellular carcinoma by spectral karyotyping.
    Wong N, Lai P, Pang E, Leung TW, Lau JW, Johnson PJ.
    Hepatology; 2000 Nov 15; 32(5):1060-8. PubMed ID: 11050057
    [Abstract] [Full Text] [Related]

  • 31. Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype.
    Bartuma H, Hallor KH, Panagopoulos I, Collin A, Rydholm A, Gustafson P, Bauer HC, Brosjö O, Domanski HA, Mandahl N, Mertens F.
    Genes Chromosomes Cancer; 2007 Jun 15; 46(6):594-606. PubMed ID: 17370328
    [Abstract] [Full Text] [Related]

  • 32. [Clinical and experimental study of 7 cases of acute lymphoblastic leukemia with dic(7;9) (pll;pll)].
    Pan JL, Xue YQ, Jiang HY, Zhu YJ, Ma L, Li TY, Wang Y, Wu YF.
    Zhonghua Xue Ye Xue Za Zhi; 2005 Aug 15; 26(8):485-8. PubMed ID: 16383241
    [Abstract] [Full Text] [Related]

  • 33. Multipoint interphase FISH in childhood T-acute lymphoblastic leukemia detects subpopulations that carry different chromosome 3 aberrations.
    Haltrich I, Kost-Alimova M, Kovács G, Dobos M, Klein G, Fekete G, Imreh S.
    Cancer Genet Cytogenet; 2007 Jan 01; 172(1):54-60. PubMed ID: 17175380
    [Abstract] [Full Text] [Related]

  • 34. Karyotypic analyses of hepatoblastoma. Report of two cases and review of the literature suggesting chromosomal loci responsible for the pathogenesis of this disease.
    Nagata T, Mugishima H, Shichino H, Suzuki T, Chin M, Koshinaga S, Inoue M, Harada K.
    Cancer Genet Cytogenet; 1999 Oct 01; 114(1):42-50. PubMed ID: 10526534
    [Abstract] [Full Text] [Related]

  • 35. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
    Kolialexi A, Kitsiou S, Fryssira H, Sofocleous C, Kouvidi E, Tsangaris GT, Salavoura K, Mavrou A.
    In Vivo; 2006 Oct 01; 20(4):473-8. PubMed ID: 16900777
    [Abstract] [Full Text] [Related]

  • 36. Fluorescence in situ hybridization: a rapid analysis to verify chromosome aberrations.
    Tocharoentanaphol C, Parinayok R, Punthuwattana N, Kangwanpong D.
    J Med Assoc Thai; 2000 Mar 01; 83 Suppl 1():S76-81. PubMed ID: 10865411
    [Abstract] [Full Text] [Related]

  • 37. Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: search for recurrent chromosome abnormalities.
    Batista DA, Vonderheid EC, Hawkins A, Morsberger L, Long P, Murphy KM, Griffin CA.
    Genes Chromosomes Cancer; 2006 Apr 01; 45(4):383-91. PubMed ID: 16382449
    [Abstract] [Full Text] [Related]

  • 38. Numerical abnormalities of chromosomes 17 and 18 in sporadic colorectal cancer: Incidence and correlation with clinical and biological findings and the prognosis of the disease.
    Garcia J, Duran A, Tabernero MD, Garcia Plaza A, Flores Corral T, Najera ML, Gomez-Alonso A, Orfao A.
    Cytometry B Clin Cytom; 2003 Jan 01; 51(1):14-20. PubMed ID: 12500293
    [Abstract] [Full Text] [Related]

  • 39. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun 01; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

  • 40. Numerical aberrations of chromosome 8 in gastric cancer detected by fluorescence in situ hybridization.
    Panani AD, Ferti AD, Avgerinos A, Raptis SA.
    Anticancer Res; 2004 Jun 01; 24(1):155-9. PubMed ID: 15015591
    [Abstract] [Full Text] [Related]

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