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Cancer Genetics and Cytogenetics|March 1, 1983
A possible specific chromosome marker for monocytic leukemia: three more patients with t(9;11)(p22;q24) and another with t(11;17)(q24;q21), each with acute monoblastic leukemiaG W Dewald, S J Morrison-DeLap, K A Schuchard, et al.Cancer Genetics and Cytogenetics|August 1, 1995
Fluorescent in situ hybridization studies of lymphocytes and neutrophils in chronic granulocytic leukemiaA Tefferi, C R Schad, R K Pruthi, et al.Cytogenetics and Cell Genetics|January 1, 1979
A tdic(5;15)(p31;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndromeG W Dewald, S J Boros, M M Conroy, et al.Cancer Genetics and Cytogenetics|October 25, 1991
Cytogenetics of six follicular thyroid adenomas including a case report of an oxyphil variant with t(8;14)(q13;q24.1)M A Herrmann, I D Hay, D H Bartelt, et al.Blood|May 23, 1998
Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemiaG W Dewald, W A Wyatt, A L Juneau, et al.Cancer Genetics and Cytogenetics|November 1, 1993
The application of fluorescent in situ hybridization to detect Mbcr/abl fusion in variant Ph chromosomes in CML and ALLG W Dewald, C R Schad, E R Christensen, et al.Cancer|September 15, 1990
Frequent occurrence of cytogenetic abnormalities in sporadic nonmedullary thyroid carcinomaR B Jenkins, I D Hay, J F Herath, et al.Pageof 2