Issue
Alert me when new journal issues are available via or via
Editorial board page CO2 Full-Text PDF (33 KB)
Original articles
Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases Valérie Beyer, Dominique Mühlematter, Valérie Parlier, Christine Cabrol, Sandrine Bougeon-Mamin, Max Solenthaler, Andreas Tobler, Paul Pugin, Michael Gregor, Felicitas Hitz, Urs Hess, Bernard Chapuis, France Laurencet, Urs Schanz, Pierre-Michel Schmidt, Guy van Melle, Martine Jotterand pages 97-119 Abstract | Full Text | Full-Text PDF (536 KB)
Losses of 1p and chromosome 14 in renal oncocytomas László Füzesi, Derk Frank, Christian Nguyen, Rolf-Hermann Ringert, Henning Bartels, Bastian Gunawan pages 120-125 Abstract | Full Text | Full-Text PDF (481 KB)
Characterization of ABCG2 gene amplification manifesting as extrachromosomal DNA in mitoxantrone-selected SF295 human glioblastoma cells V. Koneti Rao, Darawalee Wangsa, Robert W. Robey, Lyn Huff, Yasumasa Honjo, Jeffrey Hung, Turid Knutsen, Thomas Ried, Susan E. Bates pages 126-133 Abstract | Full Text | Full-Text PDF (543 KB)
Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines Deon J. Venter, Susan J. Ramus, Fleur M.A. Hammet, Melanie de Silva, Anne-Marie Hutchins, Vida Petrovic, Gareth Price, Jane E. Armes pages 134-140 Abstract | Full Text | Full-Text PDF (443 KB)
Genetic losses in breast cancer: toward an integrated molecular cytogenetic map Xin Mao, Rifat A. Hamoudi, Po Zhao, Michael Baudis pages 141-151 Abstract | Full Text | Full-Text PDF (540 KB)
Chromosome alterations in colorectal cancer in Thai patients S. Poeaim, B. Rerkamnuaychoke, S. Jesdapatarakul, A. Campiranon pages 152-159 Abstract | Full Text | Full-Text PDF (391 KB)
Short communications
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer Leandra Linhares Lacerda, Sergio Vicente Serrano, Angelo Mathes, Juan A. Rey, Maria Josefa Bello, Cacilda Casartelli pages 160-163 Abstract | Full Text | Full-Text PDF (198 KB)
Hereditary breast cancer syndromes in a Turkish population. Results of molecular germline analysis Şefik Güran, Ahmet Özet, Murat Dede, Johan J.P. Gille, Müfit Cemal Yenen pages 164-168 Abstract | Full Text | Full-Text PDF (274 KB)
No evidence of INI1hSNF5 (SMARCB1) and PARVG point mutations in oligodendroglial neoplasms M. Eva Alonso, M. Josefa Bello, Jose M. de Campos, Alberto Isla, Jesús Vaquero, Manuel Gutierrez, Jose L. Sarasa, Juan A. Rey pages 169-173 Abstract | Full Text | Full-Text PDF (242 KB)
Identification of a ring chromosome with spectral karyotyping in a pleural synovial sarcoma Jun Nishio, Hiroshi Iwasaki, Pamela A. Althof, Sabine Naumann, Masako Ishiguro, Seiji Haraoka, Akinori Iwashita, Akinori Iwasaki, Yoshio Kaku, Yasuhiko Kaneko, Masahiro Kikuchi, Julia A. Bridge pages 174-178 Abstract | Full Text | Full-Text PDF (472 KB)
Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders Ulrike Bacher, Torsten Haferlach, Claudia Schoch pages 179-183 Abstract | Full Text | Full-Text PDF (380 KB)
Deletions of the 3′ BCR and 5′ ABL regions in patients with Philadelphia-positive chronic myeloid leukemia: a one-step process occurring in about 10% of the cases without any evidence of genetic instability in the target cells Mickaël Fournier, Stéphanie Lacrosse, Mauricette Jamar, Vincent Bours, Christian Herens pages 184-187 Abstract | Full Text | Full-Text PDF (192 KB)
Prognostic significance of del(20q) in patients with hematological malignancies Jana Březinová, Zuzana Zemanová, Šárka Ransdorfová, Lenka Šindelářová, Magda Šišková, Radana Neuwirtová, Jaroslav Čermák, Kyra Michalová pages 188-192 Abstract | Full Text | Full-Text PDF (213 KB)
Frontmatter
Table of contents pages A1-A2 Full-Text PDF (38 KB)
Copyright © 2010 Elsevier, Inc. All rights reserved | Privacy Policy | Terms & Conditions | Feedback | About Us | Help | Contact Us | The content on this site is intended for health professionals.
