151 related articles for article (PubMed ID: 7664240)
1. Heterogeneity of lineage involvement by trisomy 8 in myelodysplastic syndrome. A multiparameter analysis combining conventional cytogenetics, DNA in situ hybridization, and bone marrow culture studies.
Fagioli F; Cuneo A; Bardi A; Carli MG; Bigoni R; Balsamo R; Previati R; Pazzi I; Roberti G; Rigolin GM
Cancer Genet Cytogenet; 1995 Jul; 82(2):116-22. PubMed ID: 7664240
[TBL] [Abstract][Full Text] [Related]
2. Clonal cell lineage involvement in myelodysplastic syndromes studied by fluorescence in situ hybridization and morphology.
Bernell P; Jacobsson B; Nordgren A; Hast R
Leukemia; 1996 Apr; 10(4):662-8. PubMed ID: 8618444
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic clonality in myelodysplastic syndromes studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion.
Anastasi J; Feng J; Le Beau MM; Larson RA; Rowley JD; Vardiman JW
Blood; 1993 Mar; 81(6):1580-5. PubMed ID: 8453104
[TBL] [Abstract][Full Text] [Related]
4. Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes.
Kibbelaar RE; van Kamp H; Dreef EJ; de Groot-Swings G; Kluin-Nelemans JC; Beverstock GC; Fibbe WE; Kluin PM
Blood; 1992 Apr; 79(7):1823-8. PubMed ID: 1558974
[TBL] [Abstract][Full Text] [Related]
5. Cell lineage involvement in four patients with myelodysplastic syndrome and t(1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization.
Nylund SJ; Verbeek W; Larramendy ML; Ruutu T; Heinonen K; Hallman H; Knuutila S
Cancer Genet Cytogenet; 1993 Oct; 70(2):120-4. PubMed ID: 8242591
[TBL] [Abstract][Full Text] [Related]
6. Trisomy 8 and monosomy 7 detected in bone marrow using primed in situ labeling, fluorescence in situ hybridization, and conventional cytogenetic analyses. A study of 54 cases with hematological disorders.
Yan J; Zhang XX; Fetni R; Drouin R
Cancer Genet Cytogenet; 2001 Feb; 125(1):30-40. PubMed ID: 11297765
[TBL] [Abstract][Full Text] [Related]
7. Study of clonality in myelodysplastic syndromes: detection of trisomy 8 in bone marrow cell smears by fluorescence in situ hybridization.
Abruzzese E; Buss D; Rainer R; Rao PN; Pettenati MJ
Leuk Res; 1996 Jul; 20(7):551-7. PubMed ID: 8795688
[TBL] [Abstract][Full Text] [Related]
8. Clonal CD5-positive B lymphocytes in myelodysplastic syndrome with systemic vasculitis and trisomy 8.
Billström R; Johansson B; Strömbeck B; el-Rifai W; Larramendy M; Olofsson T; Mitelman F; Knuutila S
Ann Hematol; 1997 Jan; 74(1):37-40. PubMed ID: 9031614
[TBL] [Abstract][Full Text] [Related]
9. 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; 16(9):1745-51. PubMed ID: 12200689
[TBL] [Abstract][Full Text] [Related]
10. Fluorescence in situ hybridization of progenitor cells obtained by fluorescence-activated cell sorting for the detection of cells affected by chromosome abnormality trisomy 8 in patients with myelodysplastic syndromes.
Saitoh K; Miura I; Takahashi N; Miura AB
Blood; 1998 Oct; 92(8):2886-92. PubMed ID: 9763574
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Detection of trisomy 8 by fluorescence in situ hybridization on bone marrow smears from patients with subtle myelodysplastic changes.
Brynes RK; Swayne D; McCourty A; Dosik GM; Traweek ST; Slovak ML
Arch Pathol Lab Med; 1994 Dec; 118(12):1196-200. PubMed ID: 7979913
[TBL] [Abstract][Full Text] [Related]
13. Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens.
Jenkins RB; Le Beau MM; Kraker WJ; Borell TJ; Stalboerger PG; Davis EM; Penland L; Fernald A; Espinosa R; Schaid DJ
Blood; 1992 Jun; 79(12):3307-15. PubMed ID: 1596571
[TBL] [Abstract][Full Text] [Related]
14. [Comparison of detection of trisomy 8 with fluorescence in situ hybridization and conventional karyotype analysis in myelodysplastic syndrome].
Zhang ZB; Liu SH; Li J; Bo LJ; Cui HY; Liu XP; Nie YX; Qin S
Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2002 Apr; 10(2):115-8. PubMed ID: 12513811
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?
Saumell S; Solé F; Arenillas L; Montoro J; Valcárcel D; Pedro C; Sanzo C; Luño E; Giménez T; Arnan M; Pomares H; De Paz R; Arrizabalaga B; Jerez A; Martínez AB; Sánchez-Castro J; Rodríguez-Gambarte JD; Raya JM; Ríos E; Rodríguez-Rivera M; Espinet B; Florensa L
PLoS One; 2015; 10(6):e0129375. PubMed ID: 26066831
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of trisomy 12 by fluorescence in situ hybridization in peripheral blood, bone marrow and lymph nodes of patients with B-cell chronic lymphocytic leukemia.
Liso V; Capalbo S; Lapietra A; Pavone V; Guarini A; Specchia G
Haematologica; 1999 Mar; 84(3):212-7. PubMed ID: 10189384
[TBL] [Abstract][Full Text] [Related]
17. Association between trisomy 8 and the immunophenotype of blast cells from acute leukemias secondary to a myelodysplastic syndrome or chronic myeloproliferative disorders.
Garcia-Isidoro M; Tabernero MD; Najera ML; Lopez-Berges MC; Martinez A; Durán A; Garcia JL; Hernandez JM; Garcia Marcos MA; San Miguel JF; Orfao A
Ann Hematol; 1997 May; 74(5):209-14. PubMed ID: 9200992
[TBL] [Abstract][Full Text] [Related]
18. Myelodysplastic syndrome in a child with constitutional trisomy 8 mosaicism and normal phenotype.
Hasle H; Clausen N; Pedersen B; Bendix-Hansen K
Cancer Genet Cytogenet; 1995 Jan; 79(1):79-81. PubMed ID: 7850757
[TBL] [Abstract][Full Text] [Related]
19. Hexasomy of chromosome 8 and trisomy of chromosome 11 characterize two karyotypically independent clones in a case of acute non-lymphocytic leukemia. Conventional cytogenetic and FISH investigation.
Trakhtenbrot L; Rosner E; Gipsh N; Berman S; Sofer O; Brok-Simoni F; Rechavi G; Ben-Bassat I
Cancer Genet Cytogenet; 1995 Nov; 85(1):1-4. PubMed ID: 8536231
[TBL] [Abstract][Full Text] [Related]
20. [Detection of trisomy 8 with interphase fluorescence in situ hybridization in myelodysplastic syndromes].
Li J; Pan J; Xue Y; Wu C; Xie X; Guo Y; Ruan C
Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):179-81. PubMed ID: 11876976
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
