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Cancer Genetics and Cytogenetics
Volume 159, Issue 1, Pages 1-98 (May 2005)
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Original article


Evidence for telomeric fusions as a mechanism for recurring structural aberrations of chromosome 11 in giant cell tumor of bone
Jeffrey R. Sawyer, Linda S. Goosen, Regina Lichti Binz, Charles M. Swanson, Richard W. Nicholas
pages 32-36
Abstract | Full Text | Full-Text PDF (321 KB)

Short communication


Genetic changes in localized prostate cancer of Japanese patients shown by comparative genomic hybridization
Kotaro Kasahara, Takahiro Taguchi, Ichiro Yamasaki, Masayuki Kamada, Taro Shuin
pages 84-88
Abstract | Full Text | Full-Text PDF (270 KB)


Copy number gains on 22q13 in adenoid cystic carcinoma of the salivary gland revealed by comparative genomic hybridization and tissue microarray analysis
Kolja Freier, Christa Flechtenmacher, Axel Walch, Sibylle Ohl, Frauke Devens, Bert Burke, Stefan Hassfeld, Peter Lichter, Stefan Joos, Christof Hofele
pages 89-95
Abstract | Full Text | Full-Text PDF (362 KB)

Original article


AURKA amplification, chromosome instability, and centrosome abnormality in human pancreatic carcinoma cells
Jijiang Zhu, James L. Abbruzzese, Julie Izzo, Walter N. Hittelman, Donghui Li
pages 10-17
Abstract | Full Text | Full-Text PDF (337 KB)


Molecular characterization of a consistent 4.5-megabase deletion at 4q28 in prostate cancer cells
Sei-Ichi Matsui, Jeffrey LaDuca, Michael R. Rossi, Norma J. Nowak, John K. Cowell
pages 18-26
Abstract | Full Text | Full-Text PDF (474 KB)

Short communication


Cytogenetically unrelated clones in different histologic components of a Wilms tumor
Michelle Dolan, Kristin Mascotti
pages 63-68
Abstract | Full Text | Full-Text PDF (585 KB)

Original article


Frequent allelic loss of 21q11.1∼q21.1 region in advanced stage oral squamous cell carcinoma
Lan Chen, Maria Pik Wong, Lim Kwong Cheung, Lakshman P. Samaranayake, Larry Baum, Nabil Samman
pages 37-43
Abstract | Full Text | Full-Text PDF (448 KB)

Short communication


Acquisition of a Ph chromosome with minor BCR/ABL fusion in treatment-related myelodysplastic syndrome with chromosome 7 abnormalities in a patient treated for Hodgkin disease
Abraham Kneller, Ninette Cohen, Miriam Berkowicz, Malka Reichart, Esther Rosner, Maya Sokolovski, Arnon Nagler, Gideon Rechavi, Ninette Amariglio, Luba Trakhtenbrot
pages 58-62
Abstract | Full Text | Full-Text PDF (332 KB)


A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation
Virginie Eclache, Franck Viguie, Claudie Frocrain, Bruno Cassinat, Christine Chomienne, Florence Cymbalista, Pierre Fenaux
pages 69-73
Abstract | Full Text | Full-Text PDF (265 KB)

Original article


Association between the stages of cervical cancer and chromosome 1 aneusomy
Elva I. Cortés-Gutiérrez, Martha I. Dávila-Rodríguez, Marycarmen Muraira-Rodríguez, Salvador Said-Fernández, Ricardo M. Cerda-Flores
pages 44-47
Abstract | Full Text | Full-Text PDF (160 KB)

Mini-Review


Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays
Xiaofeng Zhou, Nagesh P. Rao, Steven W. Cole, Samuel C. Mok, Zugen Chen, David T. Wong
pages 53-57
Abstract | Full Text | Full-Text PDF (234 KB)

Original article


Association of functional polymorphisms of SLC11A1 with risk of esophageal cancer in the South African Colored population
Monique G. Zaahl, Louise Warnich, Tommy C. Victor, Maritha J. Kotze
pages 48-52
Abstract | Full Text | Full-Text PDF (175 KB)

Short communication


Burkitt-type acute leukemia in a patient with B-prolymphocytic leukemia: evidence for a common origin
Florence Nguyen-Khac, Frédéric Davi, Aline Receveur, Karim Maloum, Véronique Morel, Magali Le Garff-Tavernier, Jeanne Ong, Roland Berger, Véronique Leblond, Hélène Merle-Béral
pages 74-78
Abstract | Full Text | Full-Text PDF (375 KB)

Original article


Microarray-based comparative genomic hybridization of pheochromocytoma cell lines from neurofibromatosis knockout mice reveals genetic alterations similar to those in human pheochromocytomas
James F. Powers, Arthur S. Tischler, Mansoor Mohammed, Rizwann Naeem
pages 27-31
Abstract | Full Text | Full-Text PDF (375 KB)

Lead article


A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma
Jon C. Strefford, Irina Stasevich, Tim M. Lane, Yong-Jie Lu, Tim Oliver, Bryan D. Young
pages 1-9
Abstract | Full Text | Full-Text PDF (695 KB)

Short communication


A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia
Jiyun Lee, William F. Kern, Joan B. Cain, John J. Mulvihill, Shibo Li
pages 79-83
Abstract | Full Text | Full-Text PDF (323 KB)

Letter to the editor


Variant translocation t(2;21;8)(q36;q22;q22) with RUNX1/CBFA2T1 (AML1/ETO) transcript in a case of acute myelogenous leukemia
Hui-Hua Hsiao, Goro Sashida, Atsushi Kodama, Katsuhiro Fukutake, Kazuma Ohyashiki
pages 96-97
Full Text | Full-Text PDF (145 KB)


Editorial board
page CO2
Full-Text PDF (33 KB)

Frontmatter


Table of contents
pages A1-A2
Full-Text PDF (34 KB)

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