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Clinical Genetics|March 22, 2001
Advances in the detection of chromosomal aberrations using spectral karyotypingJ Bayani, J A SquireMedical and Pediatric Oncology|February 5, 2000
Comparative genomic hybridization analysis of clear cell sarcoma of the kidneyM Barnard, J Bayani, R Grant, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|July 13, 2000
Use of multicolor spectral karyotyping in genetic analysis of pleuropulmonary blastomaM Barnard, J Bayani, R Grant, et al.Cancer Genetics and Cytogenetics|May 23, 2001
Molecular cytogenetic analysis of non-small cell lung carcinoma by spectral karyotyping and comparative genomic hybridizationC Luk, M S Tsao, J Bayani, et al.Genes, Chromosomes & Cancer|November 20, 1997
Relational mapping of MYCN and DDXI in band 2p24 and analysis of amplicon arrays in double minute chromosomes and homogeneously staining regions by use of free chromatin FISHA Pandita, R Godbout, M Zielenska, et al.Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|November 1, 1995
Application of a simplified comparative genomic hybridization technique to screen for gene amplification in pediatric solid tumorsJ Bayani, P Thorner, M Zielenska, et al.Pathology|January 22, 2000
Oncogene amplification in medulloblastoma: analysis of a case by comparative genomic hybridization and fluorescence in situ hybridizationV Jay, J Squire, J Bayani, et al.Neoplasia (New York, N.Y.)|August 10, 2000
Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcomaA Pandita, M Zielenska, P Thorner, et al.Cytogenetic and Genome Research|February 3, 2007
Correlating breakage-fusion-bridge events with the overall chromosomal instability and in vitro karyotype evolution in prostate cancerB Vukovic, B Beheshti, P Park, et al.Cytogenetic and Genome Research|June 26, 2004
Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissueS Hughes, G Lim, B Beheshti, et al.Pageof 3