Table Of Content

Cancer Genetics ANd Cytocenerics Volume 86, Number 1, January 1, 1996 Contents Original Articles Predominant 45,X,—Y Karyotype in Donor Cells After Allogeneic BMT: Cytogenetic and Molecular Analysis D. Abeliovich, O. Yehuda, A. Nagler, I. Lerer, S. Ben-Neriah, A. Amar, and R. Or A Greater Incidence of Complex Translocations in Myeloid Leukemias Than in Lymphomas and Lymphoid Leukemias Associated with IGH Rearrangement P.H. Fitzgerald and C.M. Morris Molecular Rearrangement of the MLL Gene in Adult Acute Myeloid Leukemia Without Cytogenetic Evidence of 11q23 Aberration Y.L. Kwong, R. Liang, V. Chan, and T.K. Chan Quantification of C-ERB-B, Gene Amplification in Breast Cancer Cells Using Fluorescence In Situ Hybridization and Digital Image Analysis J.L. Ferndndez, V. Goyanes, C. Lépez-Ferndndez, I. Bufio, and J. Gosdlvez Codeletion of the Genes for p16"**, Methylthioadenosine Phosphorylase, Interferon-a,, Interferon-8,, and other 9p21 Markers in Human Malignant Cell Lines H. Zhang, Z.-H. Chen, and T.M. Savarese A Case of Therapy-Related Extramedullary Acute Promyelocytic Leukemia Z. Chen, H.S. Mostafavi, D.H. Shevrin, R. Morgan, M.V. Vye, J.F. Stone, and A.A. Sandberg Acute Leukemia with t(10;11)(p11—p15;q13—q23) C. Secco, P.H. Wiernik, ].M. Bennett, and E. Paietta Translocation (Y;1)(q12;q12) in Hematologic Malignancies: Report on Two New Cases, FISH Characterization, and Review of the Literature L. Michaux, I. Wlodarska, E.R.P. Velloso, G. Verhoef, A. Van Orshoven, J.-L. Michaux, J.-M. Scheiff, C. Mecucci, and H. Van den Berghe Mapping of the Translocation Breakpoints of Primary Pleomorphic Adenomas and Lipomas Within a Common Region of Chromosome 12 S. Wanschura, G. Belge, G. Stenman, P. Kools, P. Dal Cin, E. Schoenmakers, C. Huysmans, H. Van den Berghe, S. Bartnitzke, W.J.M. Van de Ven, and J. Bullerdiek Complex Cytogenetic Rearrangement in a Case of Unicameral Bone Cyst S.A. Vayego, O.J. De Conti, and M. Varella-Garcia Chromosome Telomere Integrity of Human Solid Neoplasms M.G. Butler, M. Sciadini, L.K. Hedges, and H.S. Schwartz Chromosome Instability and Sister Chromatid Exchange (SCE) Studies in Patients with Carcinoma of Cervix Uteri V.S. Dhillon, R.S. Kler, and I.K. Dhillon Short Communications Trisomy 21 in Solitary Fibrous Tumor P. Dal Cin, R. Sciot, C.D.M. Fletcher, C. Hilliker, I. De Wever, B. Van Damme, and H. Van den Berghe Near-Hexaploid Ph-positive Acute Myeloid Leukemia with Major-BCR/ABL Transcript H. Iwama, K. Ohyashiki, ].H. Ohyashiki, T. Shimamoto, T. Fujimura, K. Kawakubo, Y. Kuriyama, A. Kodama, and K. Toyama Trisomy 11 with Loss of the Y Chromosome and Trisomy 13 in a Case of De Novo Acute Myeloid Leukemia ]. Meletis, M. Samarkos, D. Abazis, E. Michali, S. Vavourakis, E. Plata, ]. Rombos, K. Konstantopoulos, K. Pangalos, X. Yataganas, and D. Loukopoulos Contents continued on next page Contents continued A Case of Chromophobe Renal Cell Carcinoma Associated with Low Chromosome Number and Microsatellite Instability T. Shuin, K. Kondo, N. Sakai, S. Kaneko, M. Yao, Y. Nagashima, H. Kitamura, and M.A. Yoshida t(7;11) and Trilineage Myelodysplasia in Acute Myelomonocytic Leukemia T. Inaba, C. Shimazaki, S. Yoneyama, H. Hirai, T. Kikuta, T. Sumikuma, Y. Sudo, N. Yamagata, E. Ashihara, H. Goto, N. Fujita, and M. Nakagawa Presence of Three Recurrent Chromosomal Rearrangements, t(2;3)(p12;q37), del(8)(q24), and t(14;18), in an Acute Lymphoblastic Leukemia R. Berger, M. Flexor, M. Le Coniat, and C.-J. Larsen Case of Acute Monocytic Leukemia with 47,XY,+X,t(2;10)(q21.1;q26.1) and Basophilia L. Mitev, P. Apostolov, and Y. Manolova Translocation (1;5)(q32;q35) in CD30+ Anaplastic Large Cell Non-Hodgkin Lymphoma of Childhood: A Case Report L.G. Tone, R. Defavery, C.A. Scrideli, J.E. Bernardes, F.M. Torres, F.A. Soares, L. C. Peres, and M.H.O. Duarte Letters to the Editor Translocation(15;17)(q22;q21) in a Patient with Klinefelter Syndrome J.L. Garcia, J].M. Hernandez, M. Gonzalez, J.F. San Miguel, P. Dal Cin, and H. Van den Berghe Constitutional Trisomy 8 Mosaicism and Cancer H.F.L. Mark Partial Trisomy of Chromosome 4 Resulting From a Novel t(4;7) Translocation in a Case of AML M2 with Eosinophilia L.R. Hiorns, G.J. Swansbury, A. Zomas, and D. Catovsky Trisomy 8 and 20 In Desmoid Tumors and Breast Cancer: More than a Casual Coincidence? C. Rohen, S. Bartnitzke, J]. Bullerdiek, and U. Bonk Announcement Volume 86, Number 2, February 1996 Contents Original Articles Genotypic and Phenotypic Characterization of Two Newly Established Renal Cell Carcinoma Cell Lines U.S.R. Bergerheim, M. Séderhdill, E. Zabarovsky, B. Franzén, A. Manneborg-Sandlund, C. Li, S.H. Jacobson, G. Auer, G. Klein, and V.P. Collins Chromosome 1p Aberrations are Frequent in Human Primary Hepatocellular Carcinoma H.-L. Chen, Y.-C. Chen, and D.-S. Chen Near-tetraploidy in Adult Acute Myelogenous Leukemia M.R. Clarke, E.F. Lynch, L.C. Contis, M.E. Sherer, and S. Shekhter-Levin Acquisition of Doxorubicin Resistance in Human Leukemia HL-60 Cells is Reproducibly Associated with 7q21 Chromosomal Anomalies R. Ganapathi, G. Hoeltge, G. Casey, D. Grabowski, R. Neelon, and J. Ford p53 Exon 5 Mutations in Two Cases of Leukemic Mantle Cell Lymphoma D. Gandini, S. Moretti, A. Latorraca, C. De Angeli, F. Lanza, A. Cuneo, G. Castoldi, and L. del Senno Cytogenetic Survey of 53 Moroccan Patients with Acute Myeloblastic Leukemia N. Hda, B. Chadli, A. Bousfiha, A. Trachli, M. Harif, A. Benslimane Familial Association of Supernumerary Nipple with Renal Cancer K. Méhes Derivative (6)t(1;6)(q22;p21) Revealed in Bone Marrow Cells by FISH 9 Months Before Diagnosis of Acute T-Lymphoblastic Leukemia K. Michalovd, P. Lemez, O. Bartsch, J. Brezinovd, Z. Zemanovéd, J. Jelinek, I.D. Horak, and P.J. Burke Alterations of the p15, p16, and p18 Genes in Osteosarcoma C.W. Miller, A. Aslo, M.J. Campbell, N. Kawamata, B.C. Lampkin, and H.P. Koeffler Clonal Evolution of Chronic Lymphocytic Leukemia to Acute Lymphoblastic Leukemia A.N. Mohamed, R. Compean, M.E. Dan, M.R. Smith, and A. Al-Katib Cytogenetic Support for Primary Prostatic Cancer in a Patient Presenting with a Soft Tissue Mass in the Leg W.M. Molenaar, M.E.J. Stoepker, A.J. de Ruiter, H.J. Hoekstra, and E. van den Berg Constitutional de novo t(1;22)(p22;q11.2) and Ependymoma J.P. Park, S. Chaffee, W.W. Noll, and C.H. Rhodes Translocation (X;10)(p10;p10): A Rare but Nonrandom Chromosomal Abnormality in Acute Leukemia of Myeloid Differentiation K.F. Wong, K.J. Hayes, Y.O. Huh, M. Albitar, and A.B. Glassman Cytogenetic Findings in Mouse Multiple Myeloma and Waldenstrém’s Macroglobulinemia Th.W. van den Akker, J. Radl, E. Franken-Postma, and A. Hagemeijer Cytogenetic Abnormalities in 13 Patients with Multiple Myeloma F. Solé, S. Woessner, P. Acin, A. Pérez-Losada, L. Florensa, C. Besses, and J. Sans-Sabrafen Short Communications Translocation (12;15)(p13;q13) in a Patient with Relapsed Acute Myeloid Leukemia S.W. Lim, R.E. Falk, R.M. Look, M.M. Fuerst, G.N. Lawrence, D.A. Kusuanco, and F.J. Giles Isochromosome 7q in Adult Wilms’ Tumor J.A. Fletcher and A.A. Renshaw Cytogenetic Study of Extraskeletal Mesenchymal Chondrosarcoma: A case report J. Szymanska, M. Tarkkanen, T. Wiklund, M. Virolainen, C. Blomqvist, S. Asko-Seljavaara, E.Tukiainen, I. Elomaa, and S. Knuutila A Unique Clonal Chromosome 2 Deletion in Endomyometriosis A. Verhest, T. Simonart, and J.C. Noél Trisomy 21 in Acute Myeloid Leukemia C.-H. Wei, I-T. Yu, C.-H. Tzeng, F.S. Fan, R.-K. Hsieh, T.-J. Chiou, J.-H. Liu, and P.-M. Chen Letters to the Editor Detection of K-ras Mutation in a Patient With Multiple Tumors P. Kadam, P. Steele, M. Khalily, P. Miller-Canfield, and H. Preisler C-MYC Amplification in a Case of Progression from MDS to AML (M2) T. De Souza Fernandez, M.L.M. Silva, J]. De Souza, M.T.M. De Paula, and E. Abdelhay Duplication of del(20)(q1) in a Case of MDS I. Kubonishi, H. Muneishi, E. Hashimoto, N. Hatakeyama, T. Kuzume, and I. Miyoshi Volume 87, Number 1, March 1996 Contents Original Articles Incidence of Homogeneously Staining Regions in Non-Hodgkin Lymphomas E. Arranz, M. Robledo, B. Martinez, J. Gallego, A. Roman, C. Rivas, and J. Benitez t(1;5)(q23;q33) in a Patient with High-Risk B-Lineage Acute Lymphoblastic Leukemia F. Barriga, P. Bertin, E. Legiies, C. Risuefio, W. Andrade, E. Cabrera, and G. Grebe Contents continued on next page Contents continued Endoreduplication and Telomeric Association in a Choroid Plexus Carcinoma Y.S. Li, Y.-S. Fan, and R.F. Armstrong Translocation (3;3) in a Patient with Thrombocytopenia and Erythroid Dysplasia C. J. Madahar, M. Levin, J. Roy, and M. Conti Cytogenetic Characterization of the Human Prostate Cancer Cell Line P69SV40T and its Novel Tumorigenic Sublines M2182 and M15 C. Jackson-Cook, V. Bae, W. Edelman, A. Brothman, and J. Ware Sex Chromosome Abnormalities in Lung Cancer Patients B.J. Dave, V.L. Hopwood, M.R. Spitz, and S. Pathak A Mucoepidermoid Carcinoma of Minor Salivary Gland with t(11;19)(q21;p13.1) as the Only Karyotypic Abnormality A.K. El-Naggar, M. Lovell, A.M. Killary, G.L. Clayman, and ].G. Batsakis Infant Cardiac Fibroma With Clonal t(1;9)(q32;q22) and Review of Benign Fibrous Tissue Cytogenetics H.L. Ferguson, E.P. Hawkins, and L.D. Cooley Cytogenetic Findings in a Patient Presenting Simultaneously with Chronic Lymphocytic Leukemia and Acute Myeloid Leukemia M. Lima, B. Porto, M. Rodrigues, M. dos Anjos Teixeira, J. Coutinho, A.C.P. Ribeiro, ML.I. Malheiro, and B. Justi¢ga Chromosome Breakpoint at 17q11.2 and Insertion of DNA From Three Different Chromosomes in a Glioblastoma with Exceptional Glial Fibrillary Acidic Protein Expression P.E. McKeever, T.R. Dennis, A.C. Burgess, P.S. Meltzer, D.A. Marchuk, and J.M. Trent Acute Myelogenous Leukemia with dup(1)(p22p36),dup(1)(p22p36): A Novel Case? S. Porter, A.M. Walker, T.A. Lister, E.J. Watts, and D.M. Lillington t(1;19)(q23;p13) in a Case of Acute Monocytic Leukemia H.J. Weh, P. Jonveaux, D. Seeger, J. Felgner, and D.K. Hossfeld Amplification of 19q13.1-q13.2 Sequences in Ovarian Cancer: G-Band, FISH, and Molecular Studies F.H. Thompson, M.A. Nelson, J.M. Trent, X.-Y. Guan, Y. Liu, J.-M. Yang, J. Emerson, L. Adair, J. Wymer, C. Balfour, K. Massey, R. Weinstein, D.S. Alberts, and R. Taetle Aspects of the Neoplasms Observed in Patients with Constitutional Autosomal Trisomy D. Satge and H. Van Den Berghe t(4;19)(q35;q13.1): A Recurrent Change in Primitive Mesenchymal Tumors? K.E. Richkind, S.G. Romansky, and J.Z. Finklestein New Variant Ph Translocation in Chronic Myeloid Leukemia: t(Y;22)(p11;q11) M.S. Gallego, E.M. Baialardo, M. Gutierrez, M. Bonduel, and A. Feliu Short Communications del(1)(q12) in Adenocarcinomas of the Prostate H. Qi, P. Dal Cin, W. Van de Voorde, A.A. Elgamal, H. Van Poppel, L. Baert, and H. Van Den Berghe Deletion of Chromosome 20q Associated with Hypereosinophilic Syndrome: A Report of Two Cases C. Brigaudeau, E. Liozon, P. Bernard, F. Trimoreau, D. Bordessoule, and V. Praloran A New Cytogenetic Subgroup in Tenosynovial Giant Cell Tumors (Nodular Tenosynovitis) is Characterized by Involvement of 16q24 P. Dal Cin, R. Sciot, L. De Smet, B. Van Damme, and H. Van Den Berghe Aberrant Mammary Tissue and Nephrourinary Malignancy: A Man With Unilateral Polythelia and Ipsilateral Renal Adenocarcinoma Associated With Polycystic Kidney Disease C.E. Urbani and R. Betti Letters to the Editor No Rearrangement of the CHOP and TLS/FUS Genes in two Cases of Phyllodes Tumor of the Breast S.H. Birdsall, A.C. Stamps, B.A. Gusterson, J.M. Shipley, S.E. Gill, and C.S. Cooper Trisomy 13 in the Myelodysplastic Syndromes and Acute Leukemia H.F.L. Mark Announcement Volume 87, Number 2, April 1996 Contents Original Articles Fluorescence In Situ Hybridization-Based Approaches for Detection of 12p Overrepresentation, in Particular i(12p), in Cell Lines of Human Testicular Germ Cell Tumors of Adults M. M. C. Mostert, M. van de Pol, J. van Echten, D. Olde Weghuis, A. Geurts van Kessel, J. W. Oosterhuis, and L. H. J. Looijenga More Detailed Characterization of Some of the HL60 Karyotypic Features by Fluorescence In Situ Hybridization Emanuela V. Volpi, R. Vatcheva, T. Labella, and S. U. Gan High Incidence of a Second BCR-ABL Fusion in Chronic Myeloid Leukemia Revealed by Interphase Cytogenetic Analysis on Blood and Bone Marrow Smears Georges-P. Cabot, Martin Bentz, Claudia Scholl, Marion Moos, Konstanze Fischer, Peter Lichter, and Hartmut Déhner Effects of Topoisomerase II Inhibition in Lymphoblasts from Patients with Progeroid and “Chromosome Instability” Syndromes R. Elli, L. Chessa, A. Antonelli, P. Petrinelli, R. Ambra, and L. Marcucci Increased Tubulin Acetylation Accompanies Reversion to Stable Ploidy in Vincristine-Resistant CCRF-CEM Cells Melissa Geyp, Christine M. Ireland, and Sally M. Pittman Detection of Numerical Chromosome Abnormalities by FISH in Childhood Acute Lymphoblastic Leukemia Kristiina Heinonen and Eija Mahlaméki Mutagen Sensitivity in Humans: A Comparison Between Two Nomenclature Systems for Recording Chromatid Breaks T. C. Hsu, Xifeng Wu, and Zoltan Trizna Analysis of 3p Allelic Loss in Papillary and Nonpapillary Renal Cell Carcinomas: Correlation With Tumor Karyotypes Michael D. Hughson, Aurelia Meloni, Shawn Dougherty, Fred G. Silva, and Avery A. Sandberg Karyotype Evolution of the Clonal Rat Liver Cell Line CL 52 During Progression In Vitro and In Vivo Rosi Kerler and Hartmut M. Rabes Structural Aberrations of Chromosome 6 in Three Uterine Smooth Muscle Tumors Yvonne Hennig, Ulrich Deichert, Corinna Stern, Abbas Ghassemi, Brita Thode, Ulrich Bonk, Peter Meister, Sabine Bartnitzke, and Jérn Bullerdiek Significance of Clonal Chromosome Aberrations in Breast Fibroadenomas Corina Rohen, Bettina Staats, Ulrich Bonk, Sabine Bartnitzke, and Jérn Bullerdiek Unusual and Unrelated Polyclonality in a Case of Myeloid Disease A. A. Sandberg, R. Morgan, J. Betz, M. Hashimi, and M. V. Vye Metastatic Extraosseous Ewing Tumor: Association of the Additional Translocation der({16)t(1;16) with the Variant EWS/ERG Rearrangement in a Case of Cytogenetically Inconspicuous Chromosome 22 Batia Stark, Andreas Zoubek, Claudia Hattinger, Marta Jeison, Rima Gobuzov, Celia Mor, Ian Cohen, Isaac Yaniv, Peter F. Ambros, Heinrich Kovar, and Rina Zaizov Contents continued on next page Contents continued Chromosome Abnormalities in Primary Endometrioid Ovarian Carcinoma Raluca Yonescu, John L. Currie, Lora Hedrick, Janice Campbell, and Constance A. Griffin Short Communications Rearrangement of One RAR-a Gene in an Acute Promyelocytic Leukemia Case With t(15;17) and t(6;17) Involving Chromosomes 17 Band q21 E. Arranz, J. L. Lopez, M. Robledo, B. Martinez, A. Escudero, and J. Benitez Multiple Chromosome Rearrangements in a Fibrosarcoma Paola Dal Cin, Patrick Pauwels, Raf Sciot, and Herman Van Den Berghe der(16)t(1;16)(q21;q13) as a Secondary Change in Alveolar Rhabdomyosarcoma: A Case Report and Review of the Literature Aidan P. McManus, Toon Min, G. John Swansbury, Barry A. Gusterson, C. Ross Pinkerton, and Janet M. Shipley Translocation (2;3)(p13;q26) in Two Cases of Myeloid Malignancies: Acute Myeloblastic Leukemia (M2) and Blastic Phase of Chronic Myeloid Leukemia Elena W. Fleischman, Maya A. Volkova, Marina A. Frenkel, Lilia N. Konstantinova, Olga E. Kulagina, Alexander E. Baranov, and Ada A. Gordeeva Letter to the Editor Translocation (21;22)(q22;q12) in a Ewing sarcoma: New Case Characterized by Cytogenetic Analysis and Fluorescence In Situ Hybridization of a Fresh Tumor F. Mugneret, B. Favre, I. Sidaner, T. Petrella, and M. Flesh Announcements Volume 88, Number 1, May 1996 Contents Original Articles Instability of Chromosomes 1, 3, 16, and 17 in Primary Breast Carcinomas Inferred by Fluorescence In Situ Hybridization. K. Anamthawat-Jénsson, J.E. Eyfjérd, H.M. Ogmundsdéttir, I. Pétursd6éttir, and M. Steinarsdottir Detection of Genetic Alterations in Micrometastatic Cells in Bone Marrow of Cancer Patients by Fluorescence In Situ Hybridization P. Miiller, D.W eckermann, G. Riethmiiller, and G. Schlimok Cytogenetic and Histologic Correlation of Peripheral Nerve Sheath Tumors of Soft Tissue U.N.M. Rao, U. Surti, L. Hoffner, and K. Yaw Translocation (9;11;22)(p22;q23;q11): A New Type of Complex Variant Translocation of t(9;11)(p22;q23) with MLL Rearrangement N. Takahashi, I. Miura, A. Ohshima, T. Nimura, K. Hashimoto, Y. Hatano, S. Utsumi, M. Kume, K. Saito, Y. Kobayashi, M. Saito, M. Seto, R. Ueda, and A.B. Miura Spontaneous Genomic Fragility and Cell Cycle Progression in Lymphocytes of Patients With Cervical Carcinoma N. Capalash and R.C. Sobti Lack of Microsatellite Instability in Giant Cell Tumor of Bone M. Scheiner, L. Hedges, H.S. Schwartz, and M.G. Butler A Novel Reciprocal Translocation (14;15)(q11;q24) in a Congenital Mesoblastic Nephroma J.R. Sawyer, J.P. Miller, and G.J. Roloson Cytogenetic Responses to G2 Phase X-Irradiation of Cells from Retinoblastoma Patients K.K. Sanford, R. Parshad, F.M. Price, R.E. Tarone, and W.F. Benedict Translocation (X;18) in Primary Synovial Sarcoma of the Lung C.A. Roberts, T.A. Seemayer, J.R. Neff, A. Alonso, M. Nelson, and J.A. Bridge Cytogenetic Findings in Four Malignant Mixed Mesodermal Tumors of the Ovary T. Pejovic, P. Alm, S.C. Iosif, F. Mitelman, and S. Heim Cytogenetic, Cytomorphologic, and Immunologic Analysis in 55 Children with Acute Lymphoblastic Leukemia I. Petkovié, K. Josip, M. Nakié, and M. KaStelan L-MYC Allelotype in Renal Cell Carcinoma J.C. Presti, Jr., ]. Hinckley, and V.E. Reuter The Use of FISH with Chromosome-specific Repetitive DNA Probes for the Follow-up of Leukemia Patients: Correlations and Discrepancies with Bone Marrow Cytology G.J.A. Arkesteijn, S.L.A. Erpelinck, A.C.M. Martens, A. Hagemeijer, and A. Hagenbeek Inversion (14)(q11q32) in a Patient with Childhood T-Cell Acute Lymphoblastic Leukemia A. Wilkinson, D.A. Walker, N.M. Smith, A. Calvert, A.J. Monk, and C.A. Parkin The Relationship Between Age and Karyotypic Abnormalities in Myelodysplastic Syndromes K.F. Wong, K.J. Hayes, S. Leung, and A.B. Glassman Short Communications Derivative (y)t(Y;1)(q12;q12),+9 in a Patient with Polycythemia Vera During Transition into Myelodysplasia R. Raymakers, F. Stellink, and A. Geurts van Kessel Dicentric (1;15) in Myeloid Disorders L. Michaux, J. Dierlamm, C. Mecucci, P. Meeus, G. Ameye, J.-M. Libouton, G. Verhoef, A. Ferrant, A. Louwagie, C. Verellen-Dumoulin, and H. Van Den Berghe Letters to the Editor Two Additional ANLL Cases With Chromosome 3 Rearrangements Involving Bands q21 and q26 S. Borrego, G. Antifiolo, and J. Prieto Down Syndrome, Acute Lymphoblastic Leukemia, and t(8;14)(q11;q32) A.C.W. Lee, L.C. Chan, and K.W. Kwong Announcements Volume 88, Number 2, June 1996 Contents Original Articles Study on Aneuploidy and p53 Mutations in Astrocytomas P. Campomenosi, L. Ottaggio, F. Moro, S. Urbini, M. Bogliolo, A. Zunino, A. Camoriano, A. Inga, S.L. Gentile, N.S. Pellegata, S. Bonassi, E. Bruzzone, R. Iannone, R. Pisani, P. Menichini, G.N. Ranzani, S. Bonatti, A.A bbondandolo, and G. Fronza MLL/ENL Fusion in Congenital Acute Lymphoblastic Leukemia with a Unique t(11;18;19) M. Horstmann, A. Argyriou-Tirita, A. Borkhardt, H. Kabisch, P. Kapaun, K. Winkler, and O.A. Haas Long-term Follow-up of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia Patients by Polymerase Chain Reaction Analysis of Multiple Clone-specific or Malignancy-specific Gene Markers S.-q. Kuang, L.-j. Gu, S. Dong, Q. Cao, C. Xu, W. Huang, X.-Y. Su, Q.-H. Huang, J.-X. Xie, S.-J. Chen, and Z. Chen Localization of Anti-CENP Antibodies and Alphoid Sequences in Acentric Heterochromatin in a Breast Cancer Cell Line B.K. Vig, D. Latour, and M. Brown Contents continued on next page Contents continued Cytogenetic Abnormalities are Frequent in Uncultured Prostate Cancer Cells H.D. Webb, A.L. Hawkins, and C.A. Griffin No FISH Evidence for Trisomy 7 in Normal or Leukemic Bone Marrow M. Kohler, B. Johansson, S. Garwicz, S. Heim, and F. Mitelman The BAX Gene Maps to the Glioma Candidate Region at 19q13.3, but is not Altered in Human Gliomas D. Chou, T. Miyashita, H.W. Mohrenweiser, K. Ueki, K. Kastury, T. Druck, A. von Deimling, K. Huebner, J.C. Reed, and D.N. Louis Multiple Unrelated Clones in Myelodysplastic Syndrome and in Acute Myeloid Leukemia J. Musilovd, K. Michalovd, Z. Zemanovéd, and J. Brezinova Assignment of the TP53 Orthologue to a New Linkage Group (LG XIV) in Fish of the Genus Xiphophorus (Teleostei: Poeciliidae) R.S. Nairn, L. Della Coletta, B.B. McEntire, R.B. Walter, and D.C. Morizot Persistence of AML1 Rearrangement in Peripheral Blood Cells in t(8;21) Y.L. Kwong, K.F. Wong, V. Chan, and C.H. Chan FISH Studies on the Y Chromosome in Male Urinary Cells J. Betz, A.M. Meloni, and A.A. Sandberg Chromosome Changes in Nonneoplastic Tissue: Numerical and Structural Abnormalities in Nasai Polyps With Atypical Stromal Cells R. Vanni, S. Marras, A. Ravarino, G. Faa, and C. Medda Chromosomal Anomalies Exclusive of Telomeric Associations in Giant Cell Tumor of Bone E.N. McComb, S.L. Johansson, J.R. Neff, M. Nelson, and J.A. Bridge A New Translocation, t(5;21)(q13;q22) in Acute Myelogenous Leukemia S.K. Gogineni, M. da Costa, and R.S. Verma Report of a Complex Karyotype in Recurrent Metastatic Fibrolamellar Hepatocellular Carcinoma and a Review of Hepatocellular Carcinoma Cytogenetics A. Lowichik, N.R. Schneider, V. Tonk, M.Q. Ansari, and C.F. Timmons Incidence of Human Papilloma Virus in Patients With Invasive Cervical Carcinoma R.C. Sobti, N. Capalash, S. Sehgal, B.D. Gupta, and P. Sharma Short Communication Bilateral Adrenocortical Carcinoma Showing Loss of Heterozygosity at the p53 and RB Gene Loci H. Miyamoto, Y. Kubota, T. Shuin, and H. Shiozaki Letter to the Editor Common and Rare Fragile Sites on Human Chromosomes: The Cytogenetic Expression of Active and Inactive Genes? A. Musio and I. Sbrana Obituary Floyd H. Thompson (1951-1996): In Memoriam J.M. Trent, and S.E. Salmon Announcement Volume 89, Number 1, July 1, 1996 Contents Original Articles dup(10q) Lacking a-satellite DNA in Bone Marrow Cells of a Patient With Acute Myeloid Leukemia D. Abeliovich, O. Yehuda, S. Ben-Neriah, Y. Kapelushnik, and D. Ben-Yehuda Gains and Losses of DNA Sequences in Malignant Mesothelioma By Comparative Genomic Hybridization P. Kivipensas, A.-M. Bjérkqvist, R. Karhu, K. Pelin, K. Linnainmaa, L. Tammilehto, K. Mattson, O.-P. Kallioniemi, and S. Knuutila Proto-RET is Rearranged in the New Human Papillary Thyroid Cancer Cell Line PTC-1113A M.E. Herrmann Cytogenetic Analysis in Human Bone Marrow Transplantation E.M.S.F. Ribeiro, I.J. Cavalli, A.T.L. Schmid, D.A. Cornélio, A.S. Tokutake, V.M.M. Sperandio-Roxo, J.M. Rodriguez, and R. Pasquini Trisomy 15 in Hematological Malignancies: Six Cases and Review of the Literature S.R. Smith and D. Rowe Loss of Telomeric Sequences in a Ring Derived From Chromosome 8 in Refractory Anemia With Excess of Blasts in Transformation G. Fugazza, R. Bruzzone, and M. Sessarego A Nonbalanced Translocation (10;16) Demonstrated by FISH Analysis in a Case of Alveolar Adenoma of the Lung L. Roque, P. Oliveira, C. Martins, C. Carvalho, A. Serpa, and J. Soares Genotypic Characterization of a Primary Mucoepidermoid Carcinoma of the Parotid Gland By Cytogenetic, Fluorescence In Situ Hybridization, and DNA Ploidy Analysis A.K. El-Naggar, M. Lovell, A.M. Killary, and J.G. Batsakis Tetrasomy 8 in a Patient With Acute Nonlymphocytic Leukemia: A Metaphase and Interphase Study With Fluorescence in Situ Hybridization D. Mihlematter, C. Castagné, O. Bruzzese, F. Clément, P.M. Schmidt, and M.J. Bellomo Cytogenetic Analysis of Dedifferentiated Chondrosarcoma S.J. Swarts, J.R. Neff, S.L. Johansson, and J.A. Bridge Complex t(1;15;17) in Acute Promyelocytic Leukemia with Duplication of RARa and and PML Sequences J.P. Park and R.B. Fairweather Cytogenetic Investigation of Synchronous Bilateral Renal Tumors P. Dal Cin, H. Van Poppel, B. Van Damme, L. Baert, and H. Van den Berghe Loss of an X Chromosome in Aggressive Angiomyxoma of Female Soft Parts: A Case Report M.B. Kenny-Moynihan, J. Hagen, B. Richman, D.G. Mcintosh, and J.A. Bridge Renal Cell Carcinoma in an End-Stage Kidney of a Patient With a Functional Transplant: Cytogenetic and Molecular Genetic Findings M.D. Hughson, A.M. Meloni, F.G. Silva, and A.A. Sandberg Relaxation of Imprinting in Carcinogenesis M.L. Glassman, N. de Groot, and A. Hochberg Essential Thrombocythemia with BCR/ABL Rearrangement Y.L. Kwong, E.K.W. Chiu, R.H.S. Liang, V. Chan, and T.K. Chan Clinical and Cytogenetic Studies of Two Cases of Klinefelter Syndrome with Hereditary Retinoblastoma and Rhabdomyosarcoma G. Ogur, Z. Sengun, G. Arel-Kilig, C. De Busscher, S. Basaran, U. Ozbek, I. Ayan, E. Sariban, and E. Vamos Short Communications Normal Expression of fra(3)(p14.2) in Lymphocytes of Lung Cancer Patients T.S. Sundareshan and M. Augustus Extra Y Chromosome in T-cell Acute Lymphoblastic Leukemia A. Watanabe, Y. Kawachi, T. Nishihara, T. Uchida, K. Setsu, and K. Hikiji Letters to the Editor Ring Marker Containing 17q and Chromosome 22 in a Case of Dermatofibrosarcoma Protuberans N. Mandahl, J. Limon, F. Mertens, K. Arheden, and F. Mitelman Correction: Cytogenetic Findings in a Breast Stromal Sarcoma: Application of Fluorescence in Situ Hybridization to Characterize the Breakpoint Regions Contents continued on next page Contents continued in an 11;19 Translocation: Cancer Genet Cytogenet 63:47—51, 1992 LE. Garcia-Palazzo, J.P. Palazzo, Z.M. Liu, T. Taguchi, and J.R. Testa Announcement Volume 89, Number 2, July 15, 1996 Contents Original Articles Monosomy 22 in Two Ovarian Granulosa Cell Tumors V. Lindgren, S. Waggoner, and J. Rotmensch Detection of Chromosomal Abnormalities in Uterine Leiomyoma Using Conventional Cytogenetic Method and Interphase Fluorescence In Situ Hybridization S. Hayashi, N. Miharu, E. Okamoto, O. Samura, T. Hara, and K. Ohama Significance of Lymphocytic Sister Chromatid Exchange Frequencies in Ovarian Cancer Patients P.K. Dhar, S. Devi, T.R. Rao, U. Kumari, A. Joseph, M.R. Kumar, S. Nayak, Y. Shreemati, S.M. Bhat, and K.R. Bhat ider(9)(q10)t(9;22)(q34;q11) is a Recurrent Chromosomal Abnormality in Acute Lymphoblastic Leukemia and Lymphatic Blastic Phase of Chronic Myelogenous Leukemia J. Dierlamm, L. Michaux, N. Kréger, I. Wlodarska, P. Martiat, W. Zeller, D. Seeger, C. Mecucci, H. Van den Berghe, and D.K. Hossfeld Trisomy 10 in Acute Myeloid Leukemia K. Ohyashiki, A. Kodama, H. Nakamura, K.Wakasugi, H. Uchida, T. Shirota, H. Ito, and K. Toyama t(12;20)(q13;p11.2)—A New Translocation Involving the 12q13 Breakpoint in Acute Nonlymphoblastic Leukemia P. Raanani, E. Rosner, M. Bercowicz, and I. Ben-Bassat Detection of Aneuploidy in Interphase Nuclei from Non-Small Cell Lung Carcinomas by Fluorescence In Situ Hybridization Using Chromosome-Specific Repetitive DNA Probes T. Taguchi, J.-y. Zhou, M. Feder, S. Litwin, A.J.P. Klein-Szanto, and J.R. Testa Partial Deletion of the Long Arm of Chromosome 5: A Fluorescence In Situ Hybridization Study Using Band-Specific Painting Probes Generated By Chromosome Microdissection I. Tigaud, C. Charrin, R. Berger, and P. Jonveaux Evidence for Somatic Pairing of Chromosome 7 and 10 Homologs in a Follicular Lymphoma N.B. Atkin and Z. Jackson A Case of Isodicentric 7p as Sole Abnormality in a Patient With Acute Myeloid Leukemia G.C. Beverstock, P.H.E.M. de Meijer, D. ten Bokkel Huinink, J.F.M. Pruijt, G.J. den Ottolander, H.W. Wessels, and P. Mollevanger A Subtle Deletion of 12p by Routine Cytogenetics Is Found to be a Translocation to 21q by Fluorescence In Situ Hybridization: t(12;21)(p13;q22) L.V. Filatov, M. Saito, F.G. Behm, G.K. Rivera, and S.C. Raimondi Restriction Endonuclease In Situ Digestion (REISD) and Fluorescence In Situ Hybridization (FISH) as Complementary Methods to Analyze Chimerism and Residual Disease after Bone Marrow Transplantation ]. Gosdlvez, C. Lépez-Ferndndez, I. Bufio, N. Polo, P. Llamas, M.N. Ferndndez, J.L. Ferndndez, and J.L. Diez-Martin Comparative Genomic Hybridization of Germ Cell Tumors of the Adult Testis: Confirmation of Karyotypic Findings and Identification of a 12p-Amplicon M.M.C. Mostert, M. van de Pol, D. Olde Weghuis, R.F. Suijkerbuijk, A. Geurts van Kessel, J. van Echten, J.W. Oosterhuis, and L.H.J. Looijenga Detection of the Breakpoint Cluster Region-ABL Fusion in Chronic Myeloid Leukemia with Variant Philadelphia Chromosome Translocations by In Situ Hybridization S. Tosi, G. Cabot, G. Giudici, V. Attuati, P. Morandi, A. Rambaldi, H. Déhner, and A. Biondi