These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

833 related items for PubMed ID: 14716109

  • 1. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ, Antonella Z, Luisa A, Shah AD, Sheth JJ, Rocchi M.
    Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L, Parkhurst JB, Kern WF, Scott KV, Niccum D, Mulvihill JJ, Li S.
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [Abstract] [Full Text] [Related]

  • 4. Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.
    Tirado CA, Jahn JA, Scheerle J, Eid M, Meister RJ, Christie RJ, Croft CD, Wallingford S, Heritage DW, Mowrey PN, Meloni-Ehrig AM.
    Cancer Genet Cytogenet; 2005 Aug; 161(1):70-3. PubMed ID: 16080960
    [Abstract] [Full Text] [Related]

  • 5. Fluorescence in situ hybridization (FISH) in cytogenetics of leukemia.
    Michalová K.
    Folia Biol (Praha); 1996 Aug; 42(6):311-4. PubMed ID: 9158941
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [Detection of t(15;17) using cytogenetic, fluorescent in situ hybridization, and molecular techniques. Comparative study of 11 patients with acute promyelocytic leukemia].
    Arranz E, Robledo M, Martínez B, Prieto E, Román A, Benítez J.
    Sangre (Barc); 1997 Feb; 42(1):11-5. PubMed ID: 9229797
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Usefulness of cytogenetics in leukemias.
    VinSheth FJ, Sheth JJ, Patel AI, Shah AD, Verhest A.
    Indian J Cancer; 2002 Jul; 39(4):139-42. PubMed ID: 12928572
    [Abstract] [Full Text] [Related]

  • 10. Case report: acute promyelocytic leukemia with +der(17)t(15;17) detected by fluorescence in situ hybridization (FISH).
    Kim M, Lim J, Kim Y, Han K, Lee S, Min CK.
    Ann Clin Lab Sci; 2005 Jul; 35(2):195-8. PubMed ID: 15943185
    [Abstract] [Full Text] [Related]

  • 11. Molecular cytogenetic aberrations in patients with multiple myeloma studied by interphase fluorescence in situ hybridization.
    Chen L, Li J, Xu W, Qiu H, Zhu Y, Zhang Y, Duan L, Qian S, Lu H.
    Exp Oncol; 2007 Jun; 29(2):116-20. PubMed ID: 17704743
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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 01; 35(1):20-9. PubMed ID: 12203786
    [Abstract] [Full Text] [Related]

  • 14. Several chromosomes involved in translocations with chromosome 5 shown with fluorescence in situ hybridization in patients with malignant myeloid disorders.
    Bram S, Rödjer S, Swolin B.
    Cancer Genet Cytogenet; 2004 Nov 01; 155(1):74-8. PubMed ID: 15527906
    [Abstract] [Full Text] [Related]

  • 15. A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation.
    Eclache V, Viguie F, Frocrain C, Cassinat B, Chomienne C, Cymbalista F, Fenaux P.
    Cancer Genet Cytogenet; 2005 May 01; 159(1):69-73. PubMed ID: 15860361
    [Abstract] [Full Text] [Related]

  • 16. Detection of inv(16) and t(16;16) by fluorescence in situ hybridization in acute myeloid leukemia M4Eo.
    Hernández JM, González MB, Granada I, Gutiérrez N, Chillón C, Ramos F, Ribera JM, González M, Feliu E, San Miguel J.
    Haematologica; 2000 May 01; 85(5):481-5. PubMed ID: 10800163
    [Abstract] [Full Text] [Related]

  • 17. The prognostic value of FISH as an adjunct to conventional cytogenetics for the detection of cryptic gene rearrangements on chromosome 16. A retrospective investigation of 13 patients from Northern Ireland diagnosed with M4Eo acute myeloid leukaemia.
    McGrattan P, Humphreys MW.
    Ulster Med J; 2003 May 01; 72(1):16-21. PubMed ID: 12868698
    [Abstract] [Full Text] [Related]

  • 18. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
    Tosi S, Ballabio E, Teigler-Schlegel A, Boultwood J, Bruch J, Harbott J.
    Genes Chromosomes Cancer; 2005 Nov 01; 44(3):225-32. PubMed ID: 16028218
    [Abstract] [Full Text] [Related]

  • 19. Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia.
    La Starza R, Trubia M, Testoni N, Ottaviani E, Belloni E, Crescenzi B, Martelli M, Flandrin G, Pelicci PG, Mecucci C.
    Haematologica; 2002 Aug 01; 87(8):789-94. PubMed ID: 12161353
    [Abstract] [Full Text] [Related]

  • 20. Fluorescent in situ hybridization (FISH) in bone marrow and peripheral blood of leukemia patients: implications for occupational surveillance.
    McDevitt MA, Condon M, Stamberg J, Karp JE, McDiarmid M.
    Mutat Res; 2007 Apr 20; 629(1):24-31. PubMed ID: 17276720
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 42.