390 related articles for article (PubMed ID: 11165314)
1. Comparative genomic hybridization-aided unraveling of complex karyotypes in human hematopoietic neoplasias.
Verdorfer I; Brecevic L; Saul W; Schenker B; Kirsch M; Trautmann U; Helm G; Gramatzki M; Gebhart E
Cancer Genet Cytogenet; 2001 Jan; 124(1):1-6. PubMed ID: 11165314
[TBL] [Abstract][Full Text] [Related]
2. Analysis of hematologic diseases using conventional karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH).
Wilkens L; Tchinda J; Burkhardt D; Nolte M; Werner M; Georgii A
Hum Pathol; 1998 Aug; 29(8):833-9. PubMed ID: 9712425
[TBL] [Abstract][Full Text] [Related]
3. The application of comparative genomic hybridization as an additional tool in the chromosome analysis of acute myeloid leukemia and myelodysplastic syndromes.
Kim MH; Stewart J; Devlin C; Kim YT; Boyd E; Connor M
Cancer Genet Cytogenet; 2001 Apr; 126(1):26-33. PubMed ID: 11343775
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic aberrations in myelodysplastic syndrome detected by comparative genomic hybridization and fluorescence in situ hybridization.
Wilkens L; Burkhardt D; Tchinda J; Büsche G; Werner M; Nolte M; Ganser A; Georgii A
Diagn Mol Pathol; 1999 Mar; 8(1):47-53. PubMed ID: 10408793
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Comparative genomic hybridization in pediatric acute lymphoblastic leukemia.
Rice M; Breen CJ; O'Meara A; Breatnach F; O'Marcaigh AS; Stallings RL
Pediatr Hematol Oncol; 2000 Mar; 17(2):141-7. PubMed ID: 10734656
[TBL] [Abstract][Full Text] [Related]
7. Importance of using comparative genomic hybridization to improve detection of chromosomal changes in childhood acute lymphoblastic leukemia.
Jarosová M; Holzerová M; Jedlicková K; Mihál V; Zuna J; Starý J; Pospísilová D; Zemanová Z; Trka J; Blazek J; Pikalová Z; Indrák K
Cancer Genet Cytogenet; 2000 Dec; 123(2):114-22. PubMed ID: 11156736
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic aberrations in pediatric acute lymphoblastic leukemia by comparative genomic hybridization.
Karhu R; Siitonen S; Tanner M; Keinänen M; Mäkipernaa A; Lehtinen M; Vilpo JA; Isola J
Cancer Genet Cytogenet; 1997 Jun; 95(2):123-9. PubMed ID: 9169028
[TBL] [Abstract][Full Text] [Related]
10. Structural and numerical abnormalities resolved in one-step analysis: the most common chromosomal rearrangements detected by comparative genomic hybridization in childhood acute lymphoblastic leukemia.
Kowalczyk JR; Babicz M; Gaworczyk A; Lejman M; Winnicka D; Styka B; Jaszczuk I
Cancer Genet Cytogenet; 2010 Jul; 200(2):161-6. PubMed ID: 20620600
[TBL] [Abstract][Full Text] [Related]
11. Detection of chromosome over- and underrepresentations in hyperdiploid acute lymphoblastic leukemia by comparative genomic hybridization.
Wong N; Chen SJ; Cao Q; Su XY; Niu C; Wu QW; Leung TW; Wickham N; Johnson PJ; Chen Z
Cancer Genet Cytogenet; 1998 May; 103(1):20-4. PubMed ID: 9595040
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
Xu W; Li JY; Liu Q; Zhu Y; Pan JL; Qiu HR; Xue YQ
Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
[TBL] [Abstract][Full Text] [Related]
15. Interphase cytogenetics of hematological cancer: comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome specific DNA probes.
Poddighe PJ; Moesker O; Smeets D; Awwad BH; Ramaekers FC; Hopman AH
Cancer Res; 1991 Apr; 51(7):1959-67. PubMed ID: 2004382
[TBL] [Abstract][Full Text] [Related]
16. Comparative genomic hybridization is a powerful tool, complementary to cytogenetics, to identify chromosomal abnormalities in childhood acute lymphoblastic leukaemia.
Paszek-Vigier M; Talmant P; Méchinaud F; Garand R; Harousseau JL; Bataille R; Avet-Loiseau H
Br J Haematol; 1997 Dec; 99(3):589-96. PubMed ID: 9401071
[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. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.
Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP
Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582
[TBL] [Abstract][Full Text] [Related]
19. Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.
Tönnies H; Stumm M; Wegner RD; Chudoba I; Kalscheuer V; Neitzel H
Cytogenet Cell Genet; 2001; 93(3-4):188-94. PubMed ID: 11528111
[TBL] [Abstract][Full Text] [Related]
20. Complex structural involvement of chromosome 7 in primary myelodysplastic syndromes determined by fluorescence in situ hybridization.
Sessarego M; Fugazza G; Gobbi M; Bruzzone R; Bisio R; Ghio R; Patrone F
Cancer Genet Cytogenet; 1998 Oct; 106(2):110-5. PubMed ID: 9797774
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
