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Cancer Genetics and Cytogenetics page CO2 Full-Text PDF (34 KB)
Lead article
Molecular cytogenetic characterization of desmoid tumors Petter Brandal, Francesca Micci, Bodil Bjerkehagen, Mette Eknæs, Marcelo Larramendy, Ragnhild A Lothe, Sakari Knuutila, Sverre Heim pages 1-7 Abstract | Full Text | Full-Text PDF (202 KB)
Clinicopathologic significance of genetic alterations in hepatocellular carcinoma A. Pang, I.O. Ng, S.T. Fan, Y.L. Kwong pages 8-15 Abstract | Full Text | Full-Text PDF (300 KB)
Detection of amplified oncogenes by genome DNA microarrays in human primary esophageal squamous cell carcinoma: comparison with conventional comparative genomic hybridization analysis Hiroshi Arai, Takashi Ueno, Akira Tangoku, Shigefumi Yoshino, Toshihiro Abe, Shigeto Kawauchi, Atsunori Oga, Tomoko Furuya, Masaaki Oka, Kohsuke Sasaki pages 16-21 Abstract | Full Text | Full-Text PDF (291 KB)
Short communication
T-cell prolymphocytic leukemia with der(11)t(1;11)(q21;q23) and ATM deficiency Mitsuko Yamaguchi, Koh Yamamoto, Tohru Miki, Shuki Mizutani, Osamu Miura pages 22-26 Abstract | Full Text | Full-Text PDF (182 KB)
Low microsatellite instability and high loss of heterozygosity rates indicate dominant role of the suppressor pathway in squamous cell carcinoma of head and neck and loss of heterozygosity of 11q14.3 correlates with tumor grade Damjan Glavač, Metka Volavšek, Uroš Potočnik, Metka Ravnik-Glavač, Nina Gale pages 27-32 Abstract | Full Text | Full-Text PDF (281 KB)
Genetic and epigenetic alterations in sentinel lymph nodes metastatic lesions compared to their corresponding primary breast tumors Luciane R. Cavalli, Cı́cero A. Urban, Dongqiu Dai, Sônia de Assis, Denise C. Tavares, Janice D. Rone, Luiz F. Bleggi-Torres, Rubens S. Lima, Iglenir J. Cavalli, Jean-Pierre J. Issa, Bassem R. Haddad pages 33-40 Abstract | Full Text | Full-Text PDF (285 KB)
Caspase 3 and 8 deficiency in human neuroblastoma Achille Iolascon, Adriana Borriello, Lucia Giordani, Valeria Cucciolla, Arcangela Moretti, Fausta Monno, Vittoria Criniti, Andrea Marzullo, Maria Criscuolo, Fulvio Della Ragione pages 41-47 Abstract | Full Text | Full-Text PDF (232 KB)
RFP2, c13ORF1, and FAM10A4 are the most likely tumor suppressor gene candidates for B-cell chronic lymphocytic leukemia W.J van Everdink, A Baranova, C Lummen, T Tyazhelova, M.W.G Looman, D Ivanov, E Verlind, A Pestova, H Faber, A.Y van der Veen, N Yankovsky, E Vellenga, C.H.C.M Buys pages 48-57 Abstract | Full Text | Full-Text PDF (218 KB)
Identification of germline MSH2 gene mutations in endometrial cancer not fulfilling the new clinical criteria for hereditary nonpolyposis colorectal cancer Kouji Banno, Nobuyuki Susumu, Takeshi Hirao, Megumi Yanokura, Akira Hirasawa, Daisuke Aoki, Yasuhiro Udagawa, Kokichi Sugano, Shiro Nozawa pages 58-65 Abstract | Full Text | Full-Text PDF (355 KB)
Deletion (6)(p22p25) is a recurrent anomaly of thymoma: report of a second case and review of the literature Christian Herens, Marc Radermecker, Anne Servais, Pascale Quatresooz, Claire Jardon-Jeghers, Vincent Bours, Laurence de Leval pages 66-69 Abstract | Full Text | Full-Text PDF (288 KB)
Does conventional cytogenetics detect the real frequency of 19q13 aberrations in benign thyroid lesions? A survey of 38 cases Maren Meiboom, Gazanfer Belge, Silvia Bol, Chiraz El-Aouni, Eric F. Schoenmakers, Jörn Bullerdiek pages 70-72 Abstract | Full Text | Full-Text PDF (104 KB)
X chromosome inactivation in cervical cancer patients Marianne Kristiansen, Åslaug Helland, Gunnar B Kristensen, Anne O Olsen, Per E Lønning, Anne-Lise Børresen-Dale, Karen Helene Ørstavik pages 73-76 Abstract | Full Text | Full-Text PDF (88 KB)
One allele deletion of the RB1 gene in a case of refractory anemia with del(13)(q12q14): a fluorescence in situ hybridization study of the RB1 gene Fumitaka Nagamura, Tomosato Takabe, Satoshi Takahashi, Nobuhiro Ohno, Kaoru Uchimaru, Kazuo Ogami, Tohru Iseki, Arinobu Tojo, Shigetaka Asano pages 77-80 Abstract | Full Text | Full-Text PDF (177 KB)
Letter to the editor
Trisomy 8 as the sole chromosomal aberration inmyelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations Anita Heller, Lukrecija Brecevic, Melanie Glaser, Ivan Loncarevic, Erich Gebhart, Uwe Claussen, Thomas Liehr pages 81-83 Full Text | Full-Text PDF (135 KB)
Neuroblastoma in a patient with 47, XXX karyotype Davut Gül, Rı́dvan Akı́n, Erol Kı́smet, Vedat Köseoğlu pages 84-85 Full Text | Full-Text PDF (140 KB)
The apolipoprotein E ε4 allele is not a risk factor for Turkish breast cancer patients Ilhan Yaylim, Nilüfer Bozkurt, Hülya Yilmaz, Turgay Isbir, Nilgün Isik, Soykan Arikan pages 86-87 Full Text | Full-Text PDF (58 KB)
Announcement
Announcement to contributors page I Full-Text PDF (32 KB)
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