289 related articles for article (PubMed ID: 10516433)
1. Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridization.
Daniely M; Barkai G; Goldman B; Aviram-Goldring A
Cytogenet Cell Genet; 1999; 86(1):51-5. PubMed ID: 10516433
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Chromosomal rearrangements detected by FISH and G-banding.
Hou JW; Wang TR
J Formos Med Assoc; 1996 Sep; 95(9):686-91. PubMed ID: 8918057
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[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. 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]
8. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.
Fritz B; Hallermann C; Olert J; Fuchs B; Bruns M; Aslan M; Schmidt S; Coerdt W; Müntefering H; Rehder H
Eur J Hum Genet; 2001 Jul; 9(7):539-47. PubMed ID: 11464246
[TBL] [Abstract][Full Text] [Related]
9. Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
Schaeffer AJ; Chung J; Heretis K; Wong A; Ledbetter DH; Lese Martin C
Am J Hum Genet; 2004 Jun; 74(6):1168-74. PubMed ID: 15127362
[TBL] [Abstract][Full Text] [Related]
10. Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).
Benzacken B; Lapierre JM; Siffroi JP; Chalvon A; Tachdjian G
Clin Genet; 1998 Oct; 54(4):334-40. PubMed ID: 9831346
[TBL] [Abstract][Full Text] [Related]
11. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.
du Manoir S; Speicher MR; Joos S; Schröck E; Popp S; Döhner H; Kovacs G; Robert-Nicoud M; Lichter P; Cremer T
Hum Genet; 1993 Feb; 90(6):590-610. PubMed ID: 8444465
[TBL] [Abstract][Full Text] [Related]
12. FISH-microdissection (FISH-MD) analysis of complex chromosome rearrangements.
Weimer J; Kiechle M; Arnold N
Cytogenet Cell Genet; 2000; 88(1-2):114-8. PubMed ID: 10773683
[TBL] [Abstract][Full Text] [Related]
13. Comparative genomic hybridization in clinical cytogenetics.
Bryndorf T; Kirchhoff M; Rose H; Maahr J; Gerdes T; Karhu R; Kallioniemi A; Christensen B; Lundsteen C; Philip J
Am J Hum Genet; 1995 Nov; 57(5):1211-20. PubMed ID: 7485173
[TBL] [Abstract][Full Text] [Related]
14. Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.
Micci F; Teixeira MR; Heim S
Cancer Genet Cytogenet; 2001 Nov; 131(1):25-30. PubMed ID: 11734314
[TBL] [Abstract][Full Text] [Related]
15. Molecular cytogenetic characterization of Sézary syndrome.
Mao X; Lillington DM; Czepulkowski B; Russell-Jones R; Young BD; Whittaker S
Genes Chromosomes Cancer; 2003 Mar; 36(3):250-60. PubMed ID: 12557225
[TBL] [Abstract][Full Text] [Related]
16. Cytogenetic analysis by chromosome painting.
Carter NP
Cytometry; 1994 Mar; 18(1):2-10. PubMed ID: 8082483
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. DNA in situ hybridization (interphase cytogenetics) versus comparative genomic hybridization (CGH) in human cancer: detection of numerical and structural chromosome aberrations.
Van Dekken H; Krijtenburg PJ; Alers JC
Acta Histochem; 2000 Feb; 102(1):85-94. PubMed ID: 10726167
[TBL] [Abstract][Full Text] [Related]
19. Distinct cytogenetic pathways of advanced-stage neuroblastoma tumors, detected by spectral karyotyping.
Stark B; Jeison M; Bar-Am I; Glaser-Gabay L; Mardoukh J; Luria D; Feinmesser M; Goshen Y; Stein J; Abramov A; Zaizov R; Yaniv I
Genes Chromosomes Cancer; 2002 Jul; 34(3):313-24. PubMed ID: 12007192
[TBL] [Abstract][Full Text] [Related]
20. Comparative genomic hybridization in combination with flow cytometry improves results of cytogenetic analysis of spontaneous abortions.
Lomax B; Tang S; Separovic E; Phillips D; Hillard E; Thomson T; Kalousek DK
Am J Hum Genet; 2000 May; 66(5):1516-21. PubMed ID: 10741955
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]