Fluorescent in situ hybridization (FISH) in bone marrow and peripheral blood of leukemia patients: Implications for occupational surveillance von McDevitt, M.A., Condon, M., Stamberg, J., Karp, J.E., McDiarmid, M.

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Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic γδ T cell lymphoma von ALONSOZANA, E. L. C, STAMBERG, J, ABRUZZO, L. V, KUMAR, D, JAFFE, E. S, MEDEIROS, L. J, FRANTZ, C, SCHIFFER, C. A, O'CONNELL, B. A, KERMAN, S, STASS, S. A

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Repetitive Cycles of High-Dose Cytarabine Benefit Patients With Acute Myeloid Leukemia and inv(16)(p13q22) or t(16;16)(p13;q22): Results from CALGB 8461 von BYRD, John C, RUPPERT, Amy S, MAYER, Robert J, DAVEY, Frederick R, LARSON, Richard A, BLOOMFIELD, Clara D, MROZEK, Krzysztof, CARROLL, Andrew J, EDWARDS, Colin G, ARTHUR, Diane C, PETTENATI, Mark J, STAMBERG, Judith, KODURU, Prasad R. K, MOORE, Joseph O

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Outcome of Induction and Postremission Therapy in Younger Adults With Acute Myeloid Leukemia With Normal Karyotype: A Cancer and Leukemia Group B Study von FARAG, Sherif S, RUPPERT, Amy S, STAMBERG, Judith, BAER, Maria R, BLOCK, Annemarie W, VARDIMAN, James W, KOLITZ, Jonathan E, SCHIFFER, Charles A, LARSON, Richard A, BLOOMFIELD, Clara D, MROZEK, Krzysztof, MAYER, Robert J, STONE, Richard M, CARROLL, Andrew J, POWELL, Bayard L, MOORE, Joseph O, PETTENATI, Mark J, KODURU, Prasad R. K

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Patients With t(8;21)(q22;q22) and Acute Myeloid Leukemia Have Superior Failure-Free and Overall Survival When Repetitive Cycles of High-Dose Cytarabine Are Administered von BYRD, J. C, DODGE, R. K, SCHIFFER, C. A, BLOOMFIELD, C. D, CARROLL, A, BAER, M. R, EDWARDS, C, STAMBERG, J, QUMSIYEH, M, MOORE, J. O, MAYER, R. J, DAVEY, F

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Patients with isolated trisomy 8 in acute myeloid leukemia are not cured with cytarabine-based chemotherapy: results from Cancer and Leukemia Group B 8461 von BYRD, J. C, LAWRENCE, D, ARTHUR, D. C, PETTENATI, M. J, TANTRAVAHI, R, QUMSIYEH, M, STAMBERG, J, DAVEY, F. R, SCHIFFER, C. A, BLOOMFIELD, C. D

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Core binding factor acute myeloid leukemia. Cancer and Leukemia Group B (CALGB) Study 8461 von Bloomfield, C D, Ruppert, A S, Mrózek, K, Kolitz, J E, Moore, J O, Mayer, R J, Edwards, C G, Sterling, L J, Vardiman, J W, Carroll, A J, Pettenati, M J, Stamberg, J, Byrd, J C, Marcucci, G, Larson, R A

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Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization von Jalal, S. M., Law, M. E., Stamberg, J., Fonseca, R., Seely, J. R., Myers, W. H., Hanson, C. A.

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Interphase FISH for rapid identification of a Down syndrome animal model von Strovel, J., Stamberg, J., Yarowsky, P.J.

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Double minute chromosomes in monoblastic (M5) and myeloblastic (M2) acute myeloid leukemia: Two case reports and a review of literature von Thomas, Leno, Stamberg, Judith, Gojo, Ivana, Ning, Yi, Rapoport, Aaron P.

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Distinct functions of two isoforms of a homeobox gene, BP1 and DLX7, in the regulation of the β-globin gene von Fu, Sidong, Stevenson, Holly, Strovel, Jeff W., Haga, Susanne B., Stamberg, Judy, Do, Khanh, Berg, Patricia E.

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Duplication 17q mosaicism: an infant with features of Ellis-van Creveld syndrome von Serotkin, A, Stamberg, J, Waber, L

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Somatic Shift to Homozygosity for a Chromosomal Polymorphism in a Child With Acute Lymphoblastic Leukemia von Stamberg, Judith, Shende, Ashok, Lanzkowsky, Philip

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Distal monosomy 14 not associated with ring formation von Hreidarsson, S J, Stamberg, J

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Reproductive outcomes of paracentric inversion carriers: report of a liveborn dicentric recombinant and literature review von MULES, E. H, STAMBERG, J

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Chromosome abnormalities in erythroleukemia von Stamberg, Judith

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The NAD(P)H:quinone oxidoreductase locus in human colon carcinoma HCT 116 cells resistant to mitomycin C von HU, L.-T, STAMBERG, J, PAN, S.-S

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Novel translocation in acute megakaryoblastic leukemia (AML-M7) von TORETSKY, Jeffrey A, EVERLY, Eileen M, PADILLA-NASH, Hesed M, CHEN, Allen, ABRUZZO, Lynne V, ESKENAZI, Allen E, FRANTZ, Chris, RIED, Thomas, STAMBERG, Judith

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Severe growth retardation and limb anomalies in a boy with 47,XY,+r(7) and maternal uniparental disomy for chromosome 7 von Starlter, C.S., Stamberg, J., Das, S., Wulfsberg, E.A.

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Mutational analysis of natural alleles in and affecting the B incompatibility factor of Schizophyllum [commune] von Koltin, Y, Stamberg, Judith, Bawnik, N, Tamarkin, A, Werczberger, R

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