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  1. 1
    Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia

    Detection of fusion transcripts generated by the inversion 16 chromosome in acute myelogenous leukemia by David F. Claxton, P. Liu, HB Hsu, Paula Marlton, J. P. Hester, Francis S. Collins, A. B. Deisseroth, JD Rowley, MJ Siciliano

    Published 1994
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  2. 2
    Chromosomal abnormalities in Hodgkin's disease

    Chromosomal abnormalities in Hodgkin's disease by HC Schouten, WG Sanger, Michael Duggan, DD Weisenburger, KA MacLennan, JO Armitage

    Published 1989
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  3. 3
    Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes

    Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes by FA Asimakopoulos, NJ White, Elisabeth P. Nacheva, AR Green

    Published 1994
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  4. 4
    Antigen expression and polymerase chain reaction amplification of mantle cell lymphomas

    Antigen expression and polymerase chain reaction amplification of mantle cell lymphomas by RJ Molot, TC Meeker, Wittwer Ct, SL Perkins, GH Segal, AS Masih, Braylan Rc, CR Kjeldsberg

    Published 1994
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  5. 5
    Analysis of LAZ3 (BCL-6) status in B-cell non-Hodgkin's lymphomas: results of rearrangement and gene expression studies and a mutational analysis of coding region sequences

    Analysis of LAZ3 (BCL-6) status in B-cell non-Hodgkin's lymphomas: results of rearrangement and gene expression studies and a mutational analysis of coding region sequences by Takemi Otsuki, Takahiro Yano, HM Clark, Christian Bastard, JP Kerckaert, ES Jaffe, Mark Raffeld

    Published 1995
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  6. 6
    Controlling elements in the mouse X-chromosome

    Controlling elements in the mouse X-chromosome by B.M. Cattanach, J. N. Perez, C.E. Pollard

    Published 1970
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  7. 7
    Chromosome 8 breakpoint far 3′ of the c-myc oncogene in a Burkitt's lymphoma 2;8 variant translocation is equivalent to the murine pvt-1 locus.

    Chromosome 8 breakpoint far 3′ of the c-myc oncogene in a Burkitt's lymphoma 2;8 variant translocation is equivalent to the murine pvt-1 locus. by Michael W. Graham, Jerry M. Adams

    Published 1986
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  8. 8
    A novel human homeobox gene lies at the chromosome 10 breakpoint in lymphoid neoplasias with chromosomal translocation t(10;14)

    A novel human homeobox gene lies at the chromosome 10 breakpoint in lymphoid neoplasias with chromosomal translocation t(10;14) by ID Dube, Suzanne Kamel‐Reid, CC Yuan, Ming Y. Lu, X Wu, George Corpus, SC Raimondi, WM Crist, AJ Carroll, Jun Minowada

    Published 1991
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  9. 9
    Detection of the chromosomal translocation t(11;14) by polymerase chain reaction in mantle cell lymphomas

    Detection of the chromosomal translocation t(11;14) by polymerase chain reaction in mantle cell lymphomas by Ruth Rimokh, F Berger, Georges Delsol, I Digonnet, JP Rouault, JD Tigaud, Mylène Gadoux, B Coiffier, PA Bryon, JP Magaud

    Published 1994
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  10. 10
    Molecular epidemiology of Burkitt's lymphoma from South America: differences in breakpoint location and Epstein-Barr virus association from tumors in other world regions

    Molecular epidemiology of Burkitt's lymphoma from South America: differences in breakpoint location and Epstein-Barr virus association from tumors in other world regions by MI Gutiérrez, Kishor Bhatia, Francisco Barriga, Blanca Diez, FS Muriel, ML de Andreas, Sidnei Epelman, C Risueño, I T Magrath

    Published 1992
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  11. 11
    Jumping Translocations of Chromosome 1q in Multiple Myeloma: Evidence for a Mechanism Involving Decondensation of Pericentromeric Heterochromatin

    Jumping Translocations of Chromosome 1q in Multiple Myeloma: Evidence for a Mechanism Involving Decondensation of Pericentromeric Heterochromatin by Jeffrey R. Sawyer, Guido Tricot, Sandy Mattox, Sundar Jagannath, Bart Barlogie

    Published 1998
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  12. 12
    Multiple tumor-suppressor gene 1 inactivation is the most frequent genetic alteration in T-cell acute lymphoblastic leukemia

    Multiple tumor-suppressor gene 1 inactivation is the most frequent genetic alteration in T-cell acute lymphoblastic leukemia by JM Cayuela, A Madani, L Sanhes, Marc‐Henri Stern, F Sigaux

    Published 1996
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  13. 13
    Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5

    Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5 by Hélène A. Poirel, Katrina Rack, Éric Delabesse, I Radford-Weiss, Xavier Troussard, C Debert, D Leboeuf, Christian Bastard, Françoise Picard, A Veil-Buzyn, Georges Flandrin, Olivier Bernard, Elizabeth Macintyre

    Published 1996
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  14. 14
    Spontaneous abortions are reduced after preconception diagnosis of translocations.

    Spontaneous abortions are reduced after preconception diagnosis of translocations. by S. Munné, Larry E. Morrison, Jingly Fung, Carmen Márquez, Ulli Weier, Muhterem Bahçe, David Sable, Larry Grundfeld, Bill Schoolcraft, Richard T. Scott, Jacques Cohen

    Published 1998
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  15. 15
    Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys

    Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys by Nolan G. Gokey, Zhengjin Cao, Jeong W. Pak, Damian J. Lee, Susan H. McKiernan, Debbie McKenzie, Richard Weindruch, Judd M. Aiken

    Published 2004
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  16. 16
    Consistent involvement of the bcr gene by 9;22 breakpoints in pediatric acute leukemias

    Consistent involvement of the bcr gene by 9;22 breakpoints in pediatric acute leukemias by Kaveri Suryanarayan, SP Hunger, Sabine Köhler, AJ Carroll, W Crist, MP Link, ML Cleary

    Published 1991
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  17. 17
    Heterogeneity in CBF beta/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia

    Heterogeneity in CBF beta/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia by SA Shurtleff, Samuel P. Meyers, SW Hiebert, SC Raimondi, DR Head, CL Willman, S R Wolman, ML Slovak, AJ Carroll, F G Behm

    Published 1995
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  18. 18
    Nucleotide resolution analysis of <i><scp>TMPRSS2</scp></i> and <i><scp>ERG</scp></i> rearrangements in prostate cancer

    Nucleotide resolution analysis of <i><scp>TMPRSS2</scp></i> and <i><scp>ERG</scp></i> rearrangements in prostate cancer by Christopher Weier, Michael C. Haffner, Timothy L. Mosbruger, David Esopi, Jessica Hicks, Qizhi Zheng, Helen Fedor, William B. Isaacs, Angelo M. De Marzo, William G. Nelson, Srinivasan Yegnasubramanian

    Published 2013
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  19. 19
    All advanced stage non-Hodgkin's lymphomas with a polymerase chain reaction amplifiable breakpoint of bcl-2 have residual cells containing the bcl-2 rearrangement at evaluation and after treatment

    All advanced stage non-Hodgkin's lymphomas with a polymerase chain reaction amplifiable breakpoint of bcl-2 have residual cells containing the bcl-2 rearrangement at evaluation and... by JG Gribben, AS Freedman, SD Woo, K Blake, RS Shu, GJ Freeman, JA Longtine, GS Pinkus, LM Nadler

    Published 1991
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  20. 20
    Subclones with the t(9;22)/<i>BCR‐ABL1</i> rearrangement occur in AML and seem to cooperate with distinct genetic alterations

    Subclones with the t(9;22)/<i>BCR‐ABL1</i> rearrangement occur in AML and seem to cooperate with distinct genetic alterations by Ulrike Bacher, Torsten Haferlach, Tamara Alpermann, Melanie Zenger, Andreas Hochhaus, Dietrich W. Beelen, M. Uppenkamp, Mathias Rummel, Wolfgang Kern, Susanne Schnittger, Claudia Haferlach

    Published 2011
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