188 related articles for article (PubMed ID: 16010415)
1. Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia.
Karst C; Heller A; Claussen U; Gebhart E; Liehr T
Int J Oncol; 2005 Aug; 27(2):355-9. PubMed ID: 16010415
[TBL] [Abstract][Full Text] [Related]
2. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
Casas S; Aventín A; Fuentes F; Vallespí T; Granada I; Carrió A; Angel Martínez-Climent J; Solé F; Teixidó M; Bernués M; Duarte J; Maria Hernández J; Brunet S; Dolors Coll M; Sierra J
Cancer Genet Cytogenet; 2004 Aug; 153(1):16-25. PubMed ID: 15325089
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Integration of conventional cytogenetics, comparative genomic hybridisation and interphase fluorescence in situ hybridisation for the detection of genomic rearrangements in acute leukaemia.
McGrattan P; Campbell S; Cuthbert R; Jones FG; McMullin MF; Humphreys M
J Clin Pathol; 2008 Aug; 61(8):903-8. PubMed ID: 18474541
[TBL] [Abstract][Full Text] [Related]
6. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
Vranova V; Mentzlova D; Oltova A; Linkova V; Zezulkova D; Filkova H; Mendelova D; Sterba J; Kuglik P
Neoplasma; 2008; 55(1):23-30. PubMed ID: 18190236
[TBL] [Abstract][Full Text] [Related]
7. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
Mrózek K; Heinonen K; Theil KS; Bloomfield CD
Genes Chromosomes Cancer; 2002 Jun; 34(2):137-53. PubMed ID: 11979548
[TBL] [Abstract][Full Text] [Related]
8. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
Fröhling S; Kayser S; Mayer C; Miller S; Wieland C; Skelin S; Schlenk RF; Döhner H; Döhner K;
Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
[TBL] [Abstract][Full Text] [Related]
9. Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.
Cuneo A; Bigoni R; Roberti MG; Bardi A; Rigolin GM; Piva N; Mancini M; Nanni M; Alimena G; Mecucci C; Matteucci C; La Starza R; Bernasconi P; Cavigliano P; Genini E; Zaccaria A; Testoni N; Carboni C; Castoldi G
Haematologica; 1998 Jan; 83(1):21-6. PubMed ID: 9542319
[TBL] [Abstract][Full Text] [Related]
10. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
Paulsson K; Heidenblad M; Strömbeck B; Staaf J; Jönsson G; Borg A; Fioretos T; Johansson B
Leukemia; 2006 May; 20(5):840-6. PubMed ID: 16498392
[TBL] [Abstract][Full Text] [Related]
11. [Detection of abnormal numbers of chromosome 8 with interphase fluorescence in situ hybridization in hematologic malignancies].
Wang HP; Li GX; Qiao ZH; Wang HW
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):395-7. PubMed ID: 15300644
[TBL] [Abstract][Full Text] [Related]
12. Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype.
Gross M; Mkrtchyan H; Glaser M; Fricke HJ; Höffken K; Heller A; Weise A; Liehr T
Int J Oncol; 2009 Feb; 34(2):417-23. PubMed ID: 19148476
[TBL] [Abstract][Full Text] [Related]
13. Combined genetic and transcriptional profiling of acute myeloid leukemia with normal and complex karyotypes.
Lindvall C; Furge K; Björkholm M; Guo X; Haab B; Blennow E; Nordenskjöld M; Teh BT
Haematologica; 2004 Sep; 89(9):1072-81. PubMed ID: 15377468
[TBL] [Abstract][Full Text] [Related]
14. Comparison of fluorescein isothiocyanate- and Texas red-conjugated nucleotides for direct labeling in comparative genomic hybridization.
Larramendy ML; El-Rifai W; Knuutila S
Cytometry; 1998 Mar; 31(3):174-9. PubMed ID: 9515716
[TBL] [Abstract][Full Text] [Related]
15. Comparative genomic hybridization study of de novo myeloid neoplasia.
Castuma MV; Rao PH; Acevedo SH; Larripa IB
Acta Haematol; 2000; 104(1):25-30. PubMed ID: 11111118
[TBL] [Abstract][Full Text] [Related]
16. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
Karst C; Gross M; Haase D; Wedding U; Höffken K; Liehr T; Mkrtchyan H
Int J Oncol; 2006 Apr; 28(4):891-7. PubMed ID: 16525638
[TBL] [Abstract][Full Text] [Related]
17. 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; 157(2):118-26. PubMed ID: 15721632
[TBL] [Abstract][Full Text] [Related]
18. 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; 165(1):51-63. PubMed ID: 16490597
[TBL] [Abstract][Full Text] [Related]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. Fluorescence in situ hybridization reveals closely correlated results in cytological and histological specimens of hematological neoplasias compared to conventional cytogenetics.
Gerr H; Gadzicki D; Kreipe H; Schlegelberger B; Wilkens L
Pathobiology; 2006; 73(6):271-9. PubMed ID: 17374964
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
