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Editorial board page CO2 Full-Text PDF (33 KB)
Lead article
Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: leiomyosarcoma Avery A. Sandberg pages 1-19 Full Text | Full-Text PDF (466 KB)
Original articles
Loss of DNA copy number of 10q is associated with aggressive behavior of leiomyosarcomas: a comparative genomic hybridization study Jie Hu, Uma N.M. Rao, Suhagi Jasani, Vineesh Khanna, Kenneth Yaw, Urvashi Surti pages 20-27 Abstract | Full Text | Full-Text PDF (665 KB)
Establishment and characterization of a novel myxofibrosarcoma cell line Hiroyuki Kawashima, Akira Ogose, Wenguang Gu, Jun Nishio, Naoko Kudo, Naoki Kondo, Tetsuo Hotta, Hajime Umezu, Tsuyoshi Tohyama, Hirokazu Nishijima, Hiroshi Iwasaki, Naoto Endo pages 28-35 Abstract | Full Text | Full-Text PDF (628 KB)
Genome-wide aberrations in pancreatic adenocarcinoma Norma J. Nowak, Daniel Gaile, Jeffrey M. Conroy, Devin McQuaid, John Cowell, Randy Carter, Michael G. Goggins, Ralph H. Hruban, Anirban Maitra pages 36-50 Abstract | Full Text | Full-Text PDF (738 KB)
Cytogenetic characterization of a BCR-ABL transduced mouse cell line Cornelia Rudolph, Ahmed N. Hegazy, Nils von Neuhoff, Doris Steinemann, Evelin Schröck, Renata Stripecke, Christoph Klein, Brigitte Schlegelberger pages 51-56 Abstract | Full Text | Full-Text PDF (365 KB)
Analysis by comparative genomic hybridization of gastric cancer with peritoneal dissemination and/or positive peritoneal cytology Koji Morohara, Kentaro Nakao, Yusuke Tajima, Nobukazu Nishino, Kimiyasu Yamazaki, Tsutomu Kaetsu, Satoshi Suzuki, Akira Tsunoda, Masatoshi Kawamura, Tadateru Aida, Tetsuhiko Tachikawa, Mitsuo Kusano pages 57-62 Abstract | Full Text | Full-Text PDF (339 KB)
Short communications
The human ovarian teratocarcinoma cell line PA-1 demonstrates a single translocation: analysis with fluorescence in situ hybridization, spectral karyotyping, and bacterial artificial chromosome microarray Shireen Sarraf, Raphael Tejada, Massih Abawi, Michael Oberst, Tom Dennis, Kelly Claire Simon, Jan Blancato pages 63-69 Abstract | Full Text | Full-Text PDF (425 KB)
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion Carlos A. Tirado, Jennifer A. Jahn, Jay Scheerle, Maya Eid, Robert J. Meister, Robert J. Christie, Calvin D. Croft, Steven Wallingford, Deborah W. Heritage, Philip N. Mowrey, Aurelia M. Meloni-Ehrig pages 70-73 Abstract | Full Text | Full-Text PDF (259 KB)
Chronic lymphocytic leukemia developing in a patient with chronic myeloid leukemia: evidence of distinct lineage-associated genomic events Patricia Gargallo, Roberto Cacchione, Christian Chena, Juan Dupont, Guy Garay, Dardo Riveros, Irene Larripa, Irma Slavutsky pages 74-77 Abstract | Full Text | Full-Text PDF (196 KB)
Acute myelogenous leukemia with tetrasomy 8 is a disease with a poor prognosis Panagiotis Tsirigotis, Sotirios Papageorgiou, Danai Abatzis, Sofia Athanatou, Constantinos Girkas, Vasiliki Pappa, Constantinos Pangalos, Efstathios Papageorgiou, John Dervenoulas, Sotirios Raptis pages 78-81 Abstract | Full Text | Full-Text PDF (245 KB)
Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia Aurelia M. Meloni-Ehrig, Carlos A. Tirado, Kuoping Chen, Jennifer Jahn, Stephany Suchan, Jay Scheerle, Maria Gabriela Crosby, Holly Meany, Nita Seibel, David Leitenberg, Deborah W. Heritage, Philip N. Mowrey pages 82-85 Abstract | Full Text | Full-Text PDF (227 KB)
Frequent allelic imbalances at 8p and 11q22 in oral and oropharyngeal epithelial dysplastic lesions Xiaofeng Zhou, Richard C.K. Jordan, Yang Li, Bau-Lin Huang, David T.W. Wong pages 86-89 Abstract | Full Text | Full-Text PDF (192 KB)
Letters to the editor
Is the cryptic interstitial deletion of 8q24 surrounding MYC a common mechanism in the formation of double minute chromosome? Nicole C. Christacos, Leah Sherman, Alyssa Roy, Daniel J. DeAngelo, Paola Dal Cin pages 90-92 Full Text | Full-Text PDF (268 KB)
Absence of CHEK2 mutations in Spanish families with hereditary breast cancer Beatriz Bellosillo, Ignacio Tusquets, Raquel Longarón, Anna Pérez-Lezaun, Meritxell Bellet, Xavier Fabregat, Sergi Serrano, Francesc Solé pages 93-95 Full Text | Full-Text PDF (144 KB)
Frontmatter
Table of contents pages A1-A2 Full-Text PDF (33 KB)
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