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Current Protocols in Cytometry|September 5, 2008
Advanced preparative techniques to establish probes for molecular cytogeneticsJ Stap, J A Aten, D Lillington, et al.Human Molecular Genetics|July 11, 2000
The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific alu-mediated recombinationA S Hill, N J Foot, T L Chaplin, et al.Blood|September 1, 1987
Molecular analysis of relapse in chronic myeloid leukemia after allogeneic bone marrow transplantationT S Ganesan, G L Min, J M Goldman, et al.Journal of Medical Genetics|February 1, 1991
The origin of a morphologically unidentifiable human supernumerary minichromosome traced through sorting, molecular cloning, and in situ hybridisationE Raimondi, L Ferretti, B D Young, et al.Blood|June 1, 1994
Molecular cloning of two isoforms of the murine homolog of the myeloid CD33 antigenE Z Tchilian, P C Beverley, B D Young, et al.Genes, Chromosomes & Cancer|January 1, 1991
CD3G is within 200 kb of the leukemic t(4;11) translocation breakpointS Das, F E Cotter, B Gibbons, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|February 1, 1991
Direct sequence analysis of 14q+ and 18q- chromosome junctions at the MBR and MCR revealing clustering within the MBR in follicular lymphomaF E Cotter, C Price, J Meerabux, et al.Genomics|March 1, 1991
The generation of DNA probes to chromosome 11q23 by Alu PCR on small numbers of flow-sorted 22q- derivative chromosomesF E Cotter, S Das, E Douek, et al.Nucleic Acids Research|April 25, 1985
Cloning and sequence analysis of an Ig lambda light chain mRNA expressed in the Burkitt's lymphoma cell line EB4M L Anderson, L Brown, E McKenzie, et al.Human Genetics|June 1, 1987
The potential of family flow karyotyping for the detection of chromosome abnormalitiesP Harris, A Cooke, E Boyd, et al.Pageof 379