BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

105 related articles for article (PubMed ID: 2707646)

  • 1. Chromosome examinations on a six-hour culture of unstimulated peripheral blood from a patient with childhood erythroleukaemia.
    Selypes A; László A; Virág I
    Haematologia (Budap); 1989; 22(1):19-24. PubMed ID: 2707646
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Isochromosome 21 and other chromosomal abnormalities in a patient with erythroleukaemia.
    Werner-Favre C; Cabrol C; Beris P; Engel E
    Ann Genet; 1983; 26(4):240-2. PubMed ID: 6607706
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic findings in untreated patients with essential thrombocythemia.
    Panani AD
    In Vivo; 2006; 20(3):381-4. PubMed ID: 16724675
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 77(7):27-33. PubMed ID: 16116905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Monosomy 5 (-5), deletion of the long arm of chromosome 6 (6q) and acquisition of a chromosome 21 (+21) in a boy with acute leukemia at high-risk].
    Burattini MG; Santoro N; Spano M; Aufiero T; Schettini F
    Minerva Pediatr; 1989 Jul; 41(7):379-82. PubMed ID: 2601656
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between CD34 expression and chromosomal abnormalities but not clinical outcome in acute myeloid leukemia.
    Fruchart C; Lenormand B; Bastard C; Boulet D; Lesesve JF; Callat MP; Stamatoullas A; Monconduit M; Tilly H
    Am J Hematol; 1996 Nov; 53(3):175-80. PubMed ID: 8895688
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Chromosome abnormalities in acute myeloid leukemia: a cytogenetic study in an Indonesian population.
    Sudoyo AW; Indahwati ; Djoerban Z; Abdulmuthalib ; Reksodiputro AH
    Gan To Kagaku Ryoho; 2000 May; 27 Suppl 2():482-90. PubMed ID: 10895199
    [No Abstract]   [Full Text] [Related]  

  • 10. Chromosome examinations on six-hour cultures of unstimulated peripheral blood from some patients with childhood leukemia.
    Selypes A; László A
    Acta Paediatr Hung; 1990; 30(1):89-98. PubMed ID: 2317388
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Complex additional chromosomal abnormalities of del(5q), del(7q), and +22 in a patient with acute myelomonocytic leukemia carrying inv(16)].
    Nakaya A; Fujita H; Tachibana T; Takemura S; Ishigatsubo Y
    Rinsho Ketsueki; 2004 Sep; 45(9):1061-3. PubMed ID: 15510837
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic and clinical assessment of six patients with erythroleukemia.
    Trent JM; Durie BG; Davis JR; Veomett I
    Anticancer Res; 1983; 3(2):111-6. PubMed ID: 6573867
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.
    Cigudosa JC; Odero MD; Calasanz MJ; Solé F; Salido M; Arranz E; Martínez-Ramirez A; Urioste M; Alvarez S; Cervera JV; MacGrogan D; Sanz MA; Nimer SD; Benitez J
    Genes Chromosomes Cancer; 2003 Apr; 36(4):406-12. PubMed ID: 12619165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prognosis of patients with del(5q) MDS and complex karyotype and the possible role of lenalidomide in this patient subgroup.
    Giagounidis AA; Germing U; Strupp C; Hildebrandt B; Heinsch M; Aul C
    Ann Hematol; 2005 Sep; 84(9):569-71. PubMed ID: 15891887
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Correlation between cytogenetic abnormalities and disease characteristics in multiple myeloma: monosomy of chromosome 13 and structural abnormalities of 11q are associated with a high percentage of S-phase plasma cells.
    Gutiérrez NC; Hernández JM; García JL; Almeida J; Mateo G; González MI; Hernández J; Fernández-Calvo J; San Miguel JF
    Haematologica; 2000 Nov; 85(11):1146-52. PubMed ID: 11064466
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical, morphologic, and cytogenetic characteristics of 26 patients with acute erythroblastic leukemia.
    Olopade OI; Thangavelu M; Larson RA; Mick R; Kowal-Vern A; Schumacher HR; Le Beau MM; Vardiman JW; Rowley JD
    Blood; 1992 Dec; 80(11):2873-82. PubMed ID: 1450412
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Spindle cell lipoma and 13q deletion: diagnostic utility of cytogenetic analysis].
    Dumollard JM; Ranchère-Vince D; Burel F; Coindre JM; Tallini G; Ligon AH; Mayaud R; Turc-Carel C; Martin C; Mosnier JF; Pedeutour F
    Ann Pathol; 2001 Aug; 21(4):303-10. PubMed ID: 11685128
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Revision of the chromosome anomalies of the T-cell malignant cell line peer.
    Massaad L; Venuat AM; Remvikos Y; Dutrillaux B
    Ann Genet; 1990; 33(2):76-8. PubMed ID: 2241089
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic heterogeneity in erythroleukemia defined as M6 by the French-American-British (FAB) Cooperative Group criteria.
    Nakamura H
    Leukemia; 1989 Apr; 3(4):305-9. PubMed ID: 2927179
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.