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Editorial board page IFC Full-Text PDF (42 KB)
Original Articles
Cytogenetic alterations in renal tumors: a study of 38 Southeast Asian patients Lai-Ching Lau, Puay-Hoon Tan, Tsung-Wen Chong, Keng-Tatt Foo, Sidney Yip pages 1-7 Abstract | Full Text | Full-Text PDF (544 KB)
Automated Duet spot counting system and manual technologist scoring using dual-fusion fluorescence in situ hybridization (D-FISH) strategy: comparison and application to FISH minimal residual disease testing in patients with chronic myeloid leukemia Ryan A. Knudson, Brandon M. Shearer, Rhett P. Ketterling pages 8-18 Abstract | Full Text | Full-Text PDF (1128 KB)
Detection of CCND1 amplification using laser capture microdissection coupled with real-time polymerase chain reaction in human esophageal squamous cell carcinoma Chen Huang, Lin Yang, Zhongfang Li, Jun Yang, Junjie Zhao, Xu Dehui, Liying Liu, Quanli Wang, Tusheng Song pages 19-25 Abstract | Full Text | Full-Text PDF (500 KB)
Cytogenetic and molecular genetic analyses of giant cell glioblastoma multiforme reveal distinct profiles in giant cell and non-giant cell subpopulations Ramon Martinez, Wolfgang Roggendorf, Gustavo Baretton, Rüdiger Klein, Grisha Toedt, Peter Lichter, Gabriele Schackert, Stefan Joos pages 26-34 Abstract | Full Text | Full-Text PDF (281 KB)
Comparative genomic hybridization analysis of abnormalities in chromosome 21 in childhood osteosarcoma Simone dos Santos Aguiar, Lilian de Jesus Girotto Zambaldi, Adilson Manoel dos Santos, Walter Pinto, Silvia Regina Brandalise pages 35-40 Abstract | Full Text | Full-Text PDF (294 KB)
TAP1 gene polymorphisms and nasopharyngeal carcinoma risk in a Tunisian population Elham Hassen, Karim Farhat, Sallouha Gabbouj, Majida Jalbout, Noureddine Bouaouina, Lotfi Chouchane pages 41-46 Abstract | Full Text | Full-Text PDF (98 KB)
A haplotype encompassing the variant allele of DNA repair gene polymorphism ERCC2/XPD Lys751Gln but not the variant allele of Asp312Asn is associated with risk of lung cancer in a northeastern Chinese population Jiaoyang Yin, Ulla Vogel, Yegang Ma, Rong Qi, Zhongfu Sun, Huiwen Wang pages 47-51 Abstract | Full Text | Full-Text PDF (192 KB)
Short Communications
A case of chronic myeloproliferative syndrome followed by precursor T-cell acute lymphoblastic leukemia Ulrike Bacher, Torsten Haferlach, Wolfgang Kern, Hans-Detlev Harich, Susanne Schnittger, Claudia Haferlach pages 52-56 Abstract | Full Text | Full-Text PDF (846 KB)
Detection of chromosomal abnormalities in chronic lymphocytic leukemia increased by interphase fluorescence in situ hybridization in tetradecanoylphorbol acetate–stimulated peripheral blood cells Jana Sánchez, Anna Aventín pages 57-60 Abstract | Full Text | Full-Text PDF (94 KB)
The A4396G polymorphism in interferon regulatory factor 1 is frequently expressed in breast cancer cell lines Kerrie B. Bouker, Todd C. Skaar, David S. Harburger, Rebecca B. Riggins, David R. Fernandez, Alan Zwart, Robert Clarke pages 61-64 Abstract | Full Text | Full-Text PDF (92 KB)
Simultaneous translocations of FGFR3/MMSET and CCND1 into two different IGH alleles in multiple myeloma: lack of concurrent activation of both proto-oncogenes Borja Sáez, José I. Martín-Subero, Idoya Lahortiga, Cristina Largo, María J. Larrayoz, María D. Odero, Felipe Prosper, Juan C. Cigudosa, Reiner Siebert, María J. Calasanz pages 65.e1-65.e5 Abstract | Full Text | Full-Text PDF (191 KB)
KIT exon 11 deletion–inversions represent complex mutations in gastrointestinal stromal tumors Jerzy Lasota, Markku Miettinen pages 69-72 Abstract | Full Text | Full-Text PDF (125 KB)
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma Roberta La Starza, Barbara Crescenzi, Valentina Pierini, Silvia Romoli, Paolo Gorello, Lucia Brandimarte, Caterina Matteucci, Maria Grazia Kropp, Gianluca Barba, Massimo Fabrizio Martelli, Cristina Mecucci pages 73-76 Abstract | Full Text | Full-Text PDF (247 KB)
Letter to the Editor
Cryptic t(15;17) in a patient with AML M3 and a complex karyotype Gudrun Göhring, K. Lange, J. Atta, J. Krauter, D. Hölzer, B. Schlegelberger pages 77-80 Full Text | Full-Text PDF (750 KB)
A new interphase fluorescence in situ hybridization approach for genomic rearrangements involving MLH1 and MSH6 in hereditary nonpolyposis colorectal cancer-suspected mutation-negative patients Udo Koehler, Monika Grabowski, Ulrike Bacher, Elke Holinski-Feder pages 81-84 Full Text | Full-Text PDF (252 KB)
Frontmatter
Table of contents pages A1-A2 Full-Text PDF (43 KB)
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