BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 9809037)

  • 1. Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization.
    Forrest DL; Horsman DE; Jensen CL; Berry BR; Dalal BI; Barnett MJ; Nantel SH
    Cancer Genet Cytogenet; 1998 Nov; 107(1):65-8. PubMed ID: 9809037
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Refractory anaemia with hypereosinophilia and clonal abnormal metaphases detected only in the neutrophilic granulopoietic series.
    Pérez-Losada A; Woessner S; Solé F; Florensa L; Grañena A
    Acta Haematol; 1994; 91(2):80-3. PubMed ID: 8023649
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chronic myeloid leukemia associated hypereosinophilic syndrome with a clonal t(4;7)(q11;q32).
    Duell T; Mittermüller J; Schmetzer HM; Kolb HJ; Wilmanns W
    Cancer Genet Cytogenet; 1997 Apr; 94(2):91-4. PubMed ID: 9109934
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Myelodysplastic syndrome with myelofibrosis and basophilia: detection of trisomy 8 in basophils by fluorescence in-situ hybridization.
    Ma SK; Chan JC; Wan TS; Chan AY; Chan LC
    Leuk Lymphoma; 1998 Oct; 31(3-4):429-32. PubMed ID: 9869209
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Myelodysplastic syndrome (MDS) with unbalanced t(1;7) after severe aplastic anemia (SAA) in childhood as a variant form of monosomy 7.
    Kikuchi A; Ohashi H; Hanada R; Yamamoto K
    Leukemia; 1998 Dec; 12(12):2036-8. PubMed ID: 9844937
    [No Abstract]   [Full Text] [Related]  

  • 6. A novel acquired cryptic three-way translocation t(2;11;5)(p21.3;q13.5;q23.2) with a submicroscopic deletion at 11p14.3 in an adult with hypereosinophilic syndrome.
    Kjeldsen E
    Exp Mol Pathol; 2015 Aug; 99(1):50-5. PubMed ID: 25962659
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Derivative (1)t(1;16)(p11;p11.1) in myelodysplastic syndrome: a case report and review of the literature.
    Lunghi M; Casorzo L; De Paoli L; Riccomagno P; Rossi D; Gaidano G
    Cancer Genet Cytogenet; 2010 Jan; 196(1):89-92. PubMed ID: 19963141
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel chromosomal abnormality involving chromosomes 2 and 18 in a patient with myelodysplastic syndrome.
    Viniou N; Abazis D; Yataganas X; Benkhalifa M; Stamatopoulos K; Vayopoulos G; Plata E; Loukopoulos D; Pangalos C
    Cancer Genet Cytogenet; 1997 Jul; 96(1):7-12. PubMed ID: 9209462
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple copies of duplicated 1q in myelodysplastic syndrome.
    Wong KF; Wong WS
    Pathology; 2012 Jan; 44(1):57-8. PubMed ID: 22157696
    [No Abstract]   [Full Text] [Related]  

  • 10. t(5;9)(q11;q34): a novel familial translocation involving Abelson oncogene and association with hypereosinophilia.
    Bakhshi S; Hamre M; Mohamed AN; Feldman G; Ravindranath Y
    J Pediatr Hematol Oncol; 2003 Jan; 25(1):82-4. PubMed ID: 12544780
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A combination of cytomorphology, cytogenetic analysis, fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction for establishing clonality in cases of persisting hypereosinophilia.
    Bacher U; Reiter A; Haferlach T; Mueller L; Schnittger S; Kern W; Schoch C
    Haematologica; 2006 Jun; 91(6):817-20. PubMed ID: 16769584
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Quantifying chromosome changes and lineage involvement in myelodysplastic syndrome (MDS) using fluorescent in situ hybridization (FISH).
    Han K; Lee W; Harris CP; Kim W; Shim S; Meisner LF
    Leukemia; 1994 Jan; 8(1):81-6. PubMed ID: 8289503
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
    Curotti G; Benkhalifa M; Raybaud C; Picard F; Bellec V; Qumsiyeh MB
    Genet Couns; 1999; 10(3):259-64. PubMed ID: 10546097
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Dual-color FISH study on myelodysplastic syndrome with 1;7 translocation].
    Shen Y; Xue Y; Li J; Pan J; Wu Y; Guo Y; Lu D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):313-6. PubMed ID: 12170469
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Translocation t(1;7) revisited. Report of three further cases and review.
    Willem P; Pinto M; Bernstein R
    Cancer Genet Cytogenet; 1988 Nov; 36(1):45-54. PubMed ID: 3060251
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo appearance of t(7;13)(q10;q33) in the leukemic phase of myelodysplastic syndrome: a case report.
    Iguchi T; Sashida G; Kawakubo K; Tauchi T; Kodama A; Fukutake K; Ohyashiki K
    Jpn J Clin Oncol; 2002 Jan; 32(1):35-6. PubMed ID: 11932362
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Translocation (1;22) in refractory anemia and the prognostic significance of karyotypic abnormalities in refractory anemia.
    Keung YK; Cobos E; Tonk V; Morgan D
    Cancer Genet Cytogenet; 1998 Oct; 106(1):72-5. PubMed ID: 9772913
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chronic eosinophilic leukemia with 46,XY,1,der(1;7)(q10;p10) translocation.
    Park CY; Chung CH; Park YJ
    Ann Hematol; 2004 Aug; 83(8):547-8. PubMed ID: 15127233
    [No Abstract]   [Full Text] [Related]  

  • 19. Eosinophilic leukemia associated with t(2;5)(p23;q31).
    Lepretre S; Jardin F; Buchonnet G; Lenain P; Stamatoullas A; Kupfer I; Courville P; Callat MP; Contentin N; Bastard C; Tilly H
    Cancer Genet Cytogenet; 2002 Mar; 133(2):164-7. PubMed ID: 11943346
    [TBL] [Abstract][Full Text] [Related]  

  • 20. der(1)t(1;19)(p12;p11): a new nonrandom chromosomal abnormality in myelodysplastic syndrome.
    Gill JI; Varela M; Tsien F; Krause JR
    Cancer Genet Cytogenet; 1997 Apr; 94(2):85-7. PubMed ID: 9109932
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.