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

917 related items for PubMed ID: 17284364

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

  • 2. Heterogeneity of structural abnormalities in the 7q31.3 approximately q34 region in myeloid malignancies.
    González MB, Gutiérrez NC, García JL, Schoenmakers EF, Solé F, Calasanz MJ, San Miguel JF, Hernández JM.
    Cancer Genet Cytogenet; 2004 Apr 15; 150(2):136-43. PubMed ID: 15066321
    [Abstract] [Full Text] [Related]

  • 3. Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH).
    Tosi S, Harbott J, Haas OA, Douglas A, Hughes DM, Ross FM, Biondi A, Scherer SW, Kearney L.
    Leukemia; 1996 Apr 15; 10(4):644-9. PubMed ID: 8618441
    [Abstract] [Full Text] [Related]

  • 4. Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
    Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.
    Cancer Genet Cytogenet; 2006 Feb 15; 165(1):51-63. PubMed ID: 16490597
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 35(1):20-9. PubMed ID: 12203786
    [Abstract] [Full Text] [Related]

  • 6. Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype.
    Cuneo A, Bigoni R, Cavazzini F, Bardi A, Roberti MG, Agostini P, Tammiso E, Ciccone N, Mancini M, Nanni M, De Cuia R, Divona M, La Starza R, Crescenzi B, Testoni N, Rege Cambrin G, Mecucci C, Lo Coco F, Saglio G, Castoldi G.
    Leukemia; 2002 Sep 15; 16(9):1745-51. PubMed ID: 12200689
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.
    Int J Lab Hematol; 2010 Feb 15; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [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 15; 20(6):471-6. PubMed ID: 14669212
    [Abstract] [Full Text] [Related]

  • 11. Prognostic significance of del(20q) in patients with hematological malignancies.
    Brezinová J, Zemanová Z, Ransdorfová S, Sindelárová L, Sisková M, Neuwirtová R, Cermák J, Michalová K.
    Cancer Genet Cytogenet; 2005 Jul 15; 160(2):188-92. PubMed ID: 15993278
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma.
    Gazzo S, Chudoba I, Traverse-Glehen A, Baseggio L, Felman P, Berger F, Salles G, Hayette S, Magaud JP, Callet-Bauchu E.
    Cancer Genet Cytogenet; 2007 Jun 15; 175(2):159-65. PubMed ID: 17556073
    [Abstract] [Full Text] [Related]

  • 15. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y, Xu W, Liu Q, Pan J, Qiu H, Wang R, Qiao C, Jiang Y, Zhang S, Fan L, Zhang J, Shen Y, Xue Y, Li J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 15; 25(5):579-82. PubMed ID: 18841577
    [Abstract] [Full Text] [Related]

  • 16. 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 15; 29(4):299-303. PubMed ID: 18199987
    [Abstract] [Full Text] [Related]

  • 17. [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 15; 28(1):6-10. PubMed ID: 17649717
    [Abstract] [Full Text] [Related]

  • 18. [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 15; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

  • 19. Role of multiplex FISH in identifying chromosome involvement in myelodysplastic syndromes and acute myeloid leukemias with complex karyotypes: a report on 28 cases.
    Barouk-Simonet E, Soenen-Cornu V, Roumier C, Cosson A, Laï JL, Fenaux P, Preudhomme C.
    Cancer Genet Cytogenet; 2005 Mar 15; 157(2):118-26. PubMed ID: 15721632
    [Abstract] [Full Text] [Related]

  • 20. The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies.
    Chen Z, Pasquini M, Hong B, DeHart S, Heikens M, Tsai S.
    Cancer Genet Cytogenet; 2005 Oct 15; 162(2):95-8. PubMed ID: 16213355
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 46.