Showing results (1-10 of 246) with videos related to
Sort By:
Pageof 25
Genes, Chromosomes & Cancer|September 7, 2006
Analysis of genetic abnormalities provides insights into genetic evolution of hyperdiploid myelomaWee J Chng, Rhett P Ketterling, Rafael FonsecaCancer Genetics and Cytogenetics|May 15, 2007
Automated Duet spot counting system and manual technologist scoring using dual-fusion fluorescence in situ hybridization (D-FISH) strategy: comparison and application to FISH minimal residual disease testing in patients with chronic myeloid leukemiaRyan A Knudson, Brandon M Shearer, Rhett P KetterlingCancer Genetics|January 10, 2018
Myeloid neoplasm with eosinophilia associated with isolated extramedullary FIP1L1/PDGFRA rearrangementTalal Hilal, Veena Fauble, Rhett P Ketterling, et al.Cancer Genetics|August 8, 2012
When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal?Chandra Hutchens, Rhett P Ketterling, Daniel L Van DykeCancer Genetics|September 22, 2021
A rare case of atypical chronic myeloid leukemia associated with t(8;22)(p11.2;q11.2)/ BCR-FGFR1 rearrangement: A case report and literature reviewErik Washburn, Michael G Bayerl, Rhett P Ketterling, et al.Leukemia & Lymphoma|October 31, 2006
Utility of peripheral blood dual color, double fusion fluorescent in situ hybridization for BCR/ABL fusion to assess cytogenetic remission status in chronic myeloid leukemiaAndrew P Landstrom, Rhett P Ketterling, Ryan A Knudson, et al.American Journal of Clinical Pathology|November 1, 2019
Myeloid Sarcoma With CBFB-MYH11 Fusion (inv(16) or t(16;16)) Prevails in the AbdomenJoanna C Dalland, Reid Meyer, Rhett P Ketterling, et al.Cancer Genetics and Cytogenetics|August 26, 2003
New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemiaStephanie R Brockman, Sarah F Paternoster, Rhett P Ketterling, et al.British Journal of Haematology|April 2, 2005
Interphase FISH to detect PBX1/E2A fusion resulting from the der(19)t(1;19)(q23;p13.3) or t(1;19)(q23;p13.3) in paediatric patients with acute lymphoblastic leukaemiaBrandon M Shearer, Heather C Flynn, Ryan A Knudson, et al.American Journal of Medical Genetics. Part A|September 14, 2007
Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomaliesBrandon M Shearer, Erik C Thorland, Patrick R Gonzales, et al.Pageof 25