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Cancer Genetics and Cytogenetics page CO2 Full-Text PDF (33 KB)
Original article
Deletion of chromosome 15 represents a rare but recurrent chromosomal abnormality in myelocytic malignancies Judith Dierlamm, Georgia Schilling, Lucienne Michaux, Kristina Hinz, Eva Maria Murga Penas, Doris Seeger, Anne Hagemeijer, Dieter Kurt Hossfeld pages 1-5 Abstract | Full Text | Full-Text PDF (150 KB)
Loss of 1p and 7p in radiation-induced meningiomas identified by comparative genomic hybridization Evica Rajcan-Separovic, John Maguire, Tatiana Loukianova, Meimun Nisha, Dagmar Kalousek pages 6-11 Abstract | Full Text | Full-Text PDF (114 KB)
Original articles
Chromosomal gains and losses in ocular melanoma detected by comparative genomic hybridization in an Australian population-based study Claire M Vajdic, Anne-Marie Hutchins, Anne Kricker, Joanne F Aitken, Bruce K Armstrong, Nicholas K Hayward, Jane E Armes pages 12-17 Abstract | Full Text | Full-Text PDF (166 KB)
Cytogenetic characterization of three malignant peripheral nerve sheath tumors Derk Frank, Bastian Gunawan, Meike Holtrup, László Füzesi pages 18-22 Abstract | Full Text | Full-Text PDF (181 KB)
Tetrasomy 6 and 6q14 deletion are associated with better survival in hepatocellular carcinomas: a fluorescence in situ hybridization study of 77 cases Shiu-Feng Huang, Hey-Chi Hsu, Jeng-Chang Chen, Wei-Chu Chie, Polin Lai pages 23-30 Abstract | Full Text | Full-Text PDF (372 KB)
A xeno-transplantable plasma cell leukemia line with a split translocation of the IgH gene Kaneyuki Ohbayashi, Masafumi Taniwaki, Manabu Ninomiya, Hitoshi Kiyoi, Shinsuke Iida, Ryuzo Ueda, Tomoki Naoe pages 31-35 Abstract | Full Text | Full-Text PDF (258 KB)
Cytogenetics, fluorescence in situ hybridization, and reverse transcriptase polymerase chain reaction are necessary to clarify the various mechanisms leading to an MLL-AF10 fusion in acute myelocytic leukemia with 10;11 rearrangement Mirjam Klaus, Susanne Schnittger, Torsten Haferlach, Martin Dreyling, Wolfgang Hiddemann, Claudia Schoch pages 36-43 Abstract | Full Text | Full-Text PDF (287 KB)
Establishment of a new human malignant fibrous histiocytoma cell line, FU-MFH-1: cytogenetic characterization by comparative genomic hybridization and fluorescence in situ hybridization Jun Nishio, Hiroshi Iwasaki, Masako Ishiguro, Yuko Ohjimi, Noriko Nishimura, Takamasa Koga, Tatsuhiko Kawarabayashi, Yasuhiko Kaneko, Masahiro Kikuchi pages 44-51 Abstract | Full Text | Full-Text PDF (629 KB)
Arm-specific multicolor fluorescence in situ hybridization reveals widespread chromosomal instability in glioma cell lines Satu-Leena Sallinen, Pauli Sallinen, Minna Ahlstedt-Soini, Hannu Haapasalo, Heikki Helin, Jorma Isola, Ritva Karhu pages 52-60 Abstract | Full Text | Full-Text PDF (409 KB)
Short communications
Cytogenetic findings in a case of dedifferentiated chondrosarcoma Laura Casorzo, Laura Chiecchio, Alberto Pisacane, Sergio Fumero, Federico Canavese, Bruno Torchio, Mauro Risio pages 61-64 Abstract | Full Text | Full-Text PDF (280 KB)
Short communication
Monosomy 7p in meningiomas: a rare constituent of tumor progression Wolfram Henn, Isolde Niedermayer, Ralf Ketter, Sylvia Reichardt, Arno Freiler, Klaus D. Zang pages 65-68 Abstract | Full Text | Full-Text PDF (110 KB)
Trisomy 13 in a patient with common acute lymphoblastic leukemia: description of a case and review of the literature Francesca R. Spirito, Marco Mancini, Valentina Derme, Giuseppe Cimino, Anna Maria Testi, Agostino Tafuri, Antonella Vitale, Robin Foà pages 69-72 Abstract | Full Text | Full-Text PDF (125 KB)
Application of comparative genomic hybridization technique for detection of chromosomal aberrations in benign cystic teratoma A. Amiel, H. Atzmon, Z. Klein, D. Kidron, E. Gaber, O. Vassilyev, E. Shalom-Paz, A. Fishman, M.D. Fejgin pages 73-75 Abstract | Full Text | Full-Text PDF (70 KB)
An indolent B-cell lymphoma with t(2;8)(p12;q24) abnormality and absence of C-MYC amplification and TP53 deletion. A new variant? Anil Potti, Amit Panwalkar, Mark C. Ingebretson, Sugandhi A. Tharapel, Michael Goodell, M.V. Dayton, Syed A. Mehdi pages 76-79 Abstract | Full Text | Full-Text PDF (337 KB)
Evaluation of PARVG located on 22q13 as a candidate tumor suppressor gene for colorectal and breast cancer Sergi Castellvı́-Bel, Antoni Castells, Cameron N Johnstone, Virgı́nia Piñol, Maria Pellisé, Josep I Elizalde, Neus Romo, Anil K Rustgi, Josep M Piqué pages 80-82 Abstract | Full Text | Full-Text PDF (96 KB)
Letters to the editor
Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies Lihong Weng, Stefan Gesk, José I. Martı́n-Subero, Lana Harder, Brigitte Schlegelberger, Werner Grote, Reiner Siebert, Martin J.S. Dyer pages 83-84 Full Text | Full-Text PDF (96 KB)
The common fragile site FRA16C does not map within the 16q smallest region of overlap number 2 frequently lost in breast carcinoma Laurence Taine, Philippe Rocca-Serra, Azza Abd El Moneim, Nathalie Verdier, Kamran Moradkhani, Robert Saura, Philippe Gorry, Michel Longy, Françoise Bonnet pages 85-86 Full Text | Full-Text PDF (77 KB)
Letter to the editor
Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation A. Martı́nez-Ramı́rez, M. Urioste, M.J. Calasanz, J.C. Cigudosa, J. Benı́tez pages 87-89 Full Text | Full-Text PDF (272 KB)
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