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Fragile sites and bladder cancer Helen Therese Moriarty, Lucy Robyn Webster pages 89-98 Abstract | Full Text | Full-Text PDF (171 KB)
A consistent region of deletion on 1p36 in meningiomas: identification and relation to malignant progression Mamoru Murakami, Naoya Hashimoto, Yoshinobu Takahashi, Youhei Hosokawa, Johji Inazawa, Katsuyoshi Mineura pages 99-106 Abstract | Full Text | Full-Text PDF (269 KB)
Molecular cytogenetic parameters in Ewing sarcoma A. Amiel, A. Ohali, M. Fejgin, F. Sardos-Albertini, N. Bouaron, I.J. Cohen, I. Yaniv, R. Zaizov, S. Avigad pages 107-112 Abstract | Full Text | Full-Text PDF (90 KB)
Promoter hypermethylation of DLC-1, a candidate tumor suppressor gene, in several common human cancers Bao-Zhu Yuan, Marian E. Durkin, Nicholas C. Popescu pages 113-117 Abstract | Full Text | Full-Text PDF (249 KB)
Karyotypic abnormalities in myelofibrosis following polycythemia vera Joris Andrieux, Jean Loup Demory, Marie Thérèse Caulier, Philippe Agape, Marc Wetterwald, Francis Bauters, Jean Luc Laı̈ pages 118-123 Abstract | Full Text | Full-Text PDF (149 KB)
Molecular cytogenetic characterization of nasopharyngeal carcinoma cell lines and xenografts by comparative genomic hybridization and spectral karyotyping Nathalie Wong, Angela B.Y. Hui, Boli Fan, Kwok Wai Lo, Elizabeth Pang, Sing-Fai Leung, Dolly P. Huang, Philip J. Johnson pages 124-132 Abstract | Full Text | Full-Text PDF (301 KB)
Are gains of chromosomal regions 7q and 11p important abnormalities in neuroblastoma? R.L. Stallings, J. Howard, A. Dunlop, M. Mullarkey, M. McDermott, F. Breatnach, A. O'Meara pages 133-137 Abstract | Full Text | Full-Text PDF (158 KB)
A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case Ju Yan, Renaud Whittom, Robert Delage, Régen Drouin pages 138-144 Abstract | Full Text | Full-Text PDF (271 KB)
Chromosomal alterations in osteosarcoma cell lines revealed by comparative genomic hybridization and multicolor karyotyping Toshifumi Ozaki, Thomas Neumann, Daniel Wai, Karl-Ludwig Schäfer, Franz van Valen, Norbert Lindner, Christina Scheel, Werner Böcker, Winfried Winkelmann, Barbara Dockhorn-Dworniczak, Jürgen Horst, Christopher Poremba pages 145-152 Abstract | Full Text | Full-Text PDF (209 KB)
Generation of the NUP98-TOP1 fusion transcript by the t(11;20) (p15;q11) in a case of acute monocytic leukemia Suning Chen, Yongquan Xue, Zhong Chen, Yu Guo, Yafang Wu, Jinlan Pan pages 153-156 Abstract | Full Text | Full-Text PDF (118 KB)
MYCN gain and MYCN amplification in a stage 4S neuroblastoma Rosa Noguera, Adela Cañete, Antonio Pellı́n, Amparo Ruiz, Marı́a Tasso, Samuel Navarro, Victoria Castel, Antonio Llombart-Bosch pages 157-161 Abstract | Full Text | Full-Text PDF (141 KB)
Infrequent but high-level amplification of 17p11.2∼p12 in human glioma Maaike van Dartel, Sieger Leenstra, Dirk Troost, Theo J.M. Hulsebos pages 162-166 Abstract | Full Text | Full-Text PDF (215 KB)
Successful treatment with cyclosporin A of myelodysplastic syndrome with erythroid hypoplasia associated with t(6;8)(q15;q22) Shiro Takata, Kensuke Kojima, Nobuharu Fujii, Kinuyo Kaneda, Chikamasa Yoshida, Daigo Hashimoto, Shoji Asakura, Katsuji Shinagawa, Mitsune Tanimoto pages 167-169 Abstract | Full Text | Full-Text PDF (102 KB)
Trisomy 21 and other chromosomal abnormalities in acute promyelocytic leukemia T.S.K. Wan, S.K. Ma, W.Y. Au, H.S.Y. Liu, J.C.W. Chan, L.C. Chan pages 170-173 Abstract | Full Text | Full-Text PDF (113 KB)
Acute B-cell lymphoblastic leukemia with t(14;18) establishment of a new cell line Katsuyasu Saigo, Shunichi Kumagai, Mieko Kogi, Shion Imoto, Ken-ichi Hamano, Shiho Morita, Tadanobu Chinzei, Tamio Koizumi, Eiji Tatsumi pages 174-175 Full Text | Full-Text PDF (96 KB)
Minimal residual disease and trisomy 8 Francesco Pasquali, Emanuela Maserati page 176 Full Text | Full-Text PDF (44 KB)
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