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Journal Abstract Search

145 related items for PubMed ID: 7918072

  • 1. Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T-prolymphocytic leukaemia: four new cases and a review of the literature.
    Mossafa H, Brizard A, Huret JL, Brizard F, Lessard M, Guilhot F, Tanzer J.
    Br J Haematol; 1994 Apr; 86(4):780-5. PubMed ID: 7918072
    [Abstract] [Full Text] [Related]

  • 2. 14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia.
    Kojima K, Kobayashi H, Imoto S, Nakagawa T, Matsui T, Kawachi Y, Oda K, Yano T, Kobayashi H, Noguchi M, Hara M, Oshimi K.
    Int J Hematol; 1998 Oct; 68(3):291-6. PubMed ID: 9846013
    [Abstract] [Full Text] [Related]

  • 3. Inversions and tandem translocations involving chromosome 14q11 and 14q32 in T-prolymphocytic leukemia and T-cell leukemias in patients with ataxia telangiectasia.
    Brito-Babapulle V, Catovsky D.
    Cancer Genet Cytogenet; 1991 Aug; 55(1):1-9. PubMed ID: 1913594
    [Abstract] [Full Text] [Related]

  • 4. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.
    Maljaei SH, Brito-Babapulle V, Hiorns LR, Catovsky D.
    Cancer Genet Cytogenet; 1998 Jun; 103(2):110-6. PubMed ID: 9614908
    [Abstract] [Full Text] [Related]

  • 5. Cytogenetic studies on prolymphocytic leukemia. 1. B-cell prolymphocytic leukemia.
    Brito-Babapulle V, Pittman S, Melo JV, Pomfret M, Catovsky D.
    Hematol Pathol; 1987 Jun; 1(1):27-33. PubMed ID: 3509770
    [Abstract] [Full Text] [Related]

  • 6. Deletions of D13S25, D13S319 and RB-1 mapping to 13q14.3 in T-cell prolymphocytic leukaemia.
    Brito-Babapulle V, Baou M, Matutes E, Morilla R, Atkinson S, Catovsky D.
    Br J Haematol; 2001 Aug; 114(2):327-32. PubMed ID: 11529851
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  • 7. High levels of chromosomal imbalances in typical and small-cell variants of T-cell prolymphocytic leukemia.
    Costa D, Queralt R, Aymerich M, Carrió A, Rozman M, Vallespí T, Colomer D, Nomdedeu B, Montserrat E, Campo E.
    Cancer Genet Cytogenet; 2003 Nov; 147(1):36-43. PubMed ID: 14580769
    [Abstract] [Full Text] [Related]

  • 8. Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
    Dürig J, Bug S, Klein-Hitpass L, Boes T, Jöns T, Martin-Subero JI, Harder L, Baudis M, Dührsen U, Siebert R.
    Leukemia; 2007 Oct; 21(10):2153-63. PubMed ID: 17713554
    [Abstract] [Full Text] [Related]

  • 9. Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia.
    Espinet B, Solé F, Salido M, Lloveras E, Abella E, Besses C, Serrano S, Woessner S, Florensa L.
    Haematologica; 2000 Jun; 85(6):607-12. PubMed ID: 10870117
    [Abstract] [Full Text] [Related]

  • 10. Cytogenetic studies on prolymphocytic leukemia. II. T cell prolymphocytic leukemia.
    Brito-Babapulle V, Pomfret M, Matutes E, Catovsky D.
    Blood; 1987 Oct; 70(4):926-31. PubMed ID: 3115337
    [Abstract] [Full Text] [Related]

  • 11. Expression of c-myc oncoprotein in chronic T cell leukemias.
    Maljaie SH, Brito-Babapulle V, Matutes E, Hiorns LR, De Schouwer PJ, Catovsky D.
    Leukemia; 1995 Oct; 9(10):1694-9. PubMed ID: 7564512
    [Abstract] [Full Text] [Related]

  • 12. [Cutaneous localization of T-cell prolymphocytic leukemia].
    Thomas A, Dompmartin A, Troussard X, Moreau A, Manard C, Leroy D.
    Ann Dermatol Venereol; 1995 Oct; 122(8):526-9. PubMed ID: 8572493
    [Abstract] [Full Text] [Related]

  • 13. Relationship of T leukaemias with cerebriform nuclei to T-prolymphocytic leukaemia: a cytogenetic analysis with in situ hybridization.
    Brito-Babapulle V, Maljaie SH, Matutes E, Hedges M, Yuille M, Catovsky D.
    Br J Haematol; 1997 Mar; 96(4):724-32. PubMed ID: 9074412
    [Abstract] [Full Text] [Related]

  • 14. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J, Pierron G, Vecchione D, Garand R, Brizard F, Sigaux F, Stern MH, Aurias A.
    Genes Chromosomes Cancer; 2001 Jul; 31(3):248-54. PubMed ID: 11391795
    [Abstract] [Full Text] [Related]

  • 15. Unusual breakpoint distribution of 8p abnormalities in T-prolymphocytic leukemia: a study with YACS mapping to 8p11-p12.
    Sorour A, Brito-Babapulle V, Smedley D, Yuille M, Catovsky D.
    Cancer Genet Cytogenet; 2000 Sep; 121(2):128-32. PubMed ID: 11063795
    [Abstract] [Full Text] [Related]

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  • 17. Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.
    Put N, Van Roosbroeck K, Konings P, Meeus P, Brusselmans C, Rack K, Gervais C, Nguyen-Khac F, Chapiro E, Radford-Weiss I, Struski S, Dastugue N, Gachard N, Lefebvre C, Barin C, Eclache V, Fert-Ferrer S, Laibe S, Mozziconacci MJ, Quilichini B, Poirel HA, Wlodarska I, Hagemeijer A, Moreau Y, Vandenberghe P, Michaux L, BCGHo and the GFCH.
    Ann Hematol; 2012 Jun; 91(6):863-73. PubMed ID: 22205151
    [Abstract] [Full Text] [Related]

  • 18. Multiple karyotypic abnormalities in three cases of small cell variant of T-cell prolymphocytic leukemia.
    Heinonen K, Mahlamäki E, Hämäläinen E, Nousiainen T, Mononen I.
    Cancer Genet Cytogenet; 1994 Nov; 78(1):28-35. PubMed ID: 7987802
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