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British Journal of Haematology|May 31, 2001
Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasiaA Tefferi, R A Mesa, G Schroeder, et al.
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.
Mayo Clinic Proceedings|November 1, 1994
Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemiaC R Schad, C A Hanson, E Paietta, et al.
Blood|February 15, 1993
The 5q- syndrome: a single-institution study of 43 consecutive patientsP Mathew, A Tefferi, G W Dewald, et al.
American Journal of Clinical Pathology|June 30, 2000
The (11;14)(q13;q32) translocation in multiple myeloma. A morphologic and immunohistochemical studyJ D Hoyer, C A Hanson, R Fonseca, 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.
Blood|September 25, 1998
A special fluorescent in situ hybridization technique to study peripheral blood and assess the effectiveness of interferon therapy in chronic myeloid leukemiaI Buño, W A Wyatt, A R Zinsmeister, et al.
Mayo Clinic Proceedings|February 1, 1989
Cytogenetic studies in 11 patients with small cell carcinoma of the lungP A De Fusco, S Frytak, R J Dahl, et al.
Annals of Neurology|May 1, 1992
Prognostic value of cytogenetic analysis in human cerebral astrocytomasD W Kimmel, J R O'Fallon, B W Scheithauer, 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.
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