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Human Pathology|February 1, 1997
Relevance of cytogenetic and fluorescent in situ hybridization analyses in the clinical assessment of soft tissue sarcomaG Sozzi, F Minoletti, M Miozzo, et al.Cancer Genetics and Cytogenetics|July 1, 1987
Chromosomal abnormalities in a primary small cell lung cancerG Sozzi, M G Bertoglio, M G Borrello, et al.JAMA|December 26, 2001
Potential cancer therapy with the fragile histidine triad gene: review of the preclinical studiesH Ishii, K R Dumon, A Vecchione, et al.Cancer Research|July 15, 1991
Chromosome locations of the MYB related genes, AMYB and BMYBC Barletta, T Druck, S LaForgia, et al.Cancer Genetics and Cytogenetics|August 1, 1995
A novel t(9;11)(p22;q23) with ALL-1 gene rearrangement associated with progression of a myeloproliferative disorder to acute myeloid leukemiaM Negrini, A Cuneo, T Nakamura, et al.Cancer Research|July 1, 1993
Common region of ALL-1 gene disrupted in epipodophyllotoxin-related secondary acute myeloid leukemiaC A Felix, N J Winick, M Negrini, et al.Cancer Research|July 15, 1996
The FHIT gene at 3p14.2 is abnormal in breast carcinomasM Negrini, C Monaco, I Vorechovsky, et al.Cancer Research|October 1, 1993
Potential topoisomerase II DNA-binding sites at the breakpoints of a t(9;11) chromosome translocation in acute myeloid leukemiaM Negrini, C A Felix, C Martin, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1979
Chromosomal location of the genes for human immunoglobulin heavy chainsC M Croce, M Shander, J Martinis, et al.Nature|February 7, 1985
Suppression of the normal mouse c-myc oncogene in human lymphoma cellsS Feo, A ar-Rushdi, K Huebner, et al.Pageof 60