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Cancer Genetics and Cytogenetics
Volume 167, Issue 1, Pages 1-96 (May 2006)
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Editorial board
page CO2
Full-Text PDF (42 KB)

Original articles


Allele-specific loss of heterozygosity in multiple colorectal adenomas: toward an integrated molecular cytogenetic map II
Xin Mao, Rifat A. Hamoudi, Ian C. Talbot, Michael Baudis
pages 1-14
Abstract | Full Text | Full-Text PDF (461 KB)


Transitional cell bladder tumor: predicting recurrence and progression by analysis of microsatellite loss of heterozygosity in urine sediment and tumor tissue
Delfina Fornari, Kenneth Steven, Alastair B. Hansen, Jan V. Jepsen, Asger L. Poulsen, Henrik Vibits, Thomas Horn
pages 15-19
Abstract | Full Text | Full-Text PDF (166 KB)


Chromosomal aberrations in 130 patients with multiple myeloma studied by interphase FISH: diagnostic and prognostic relevance
I.G.H. Schmidt-Wolf, A. Glasmacher, C. Hahn-Ast, A. Jüttner, T. Schnurr, F. Cremer, T. Moehler, H. Goldschmidt, B. Busert, R. Schubert, G. Schwanitz
pages 20-25
Abstract | Full Text | Full-Text PDF (321 KB)


Evaluation of microsatellite amplifications at chromosomal locus 3q26 as surrogate marker for premalignant changes in mucosa surrounding head and neck squamous cell carcinoma
Jürgen Brieger, Jan Kastner, Jan Gosepath, Wolf J. Mann
pages 26-31
Abstract | Full Text | Full-Text PDF (317 KB)


Allelic imbalance of HER2 variant in sporadic breast and ovarian cancer
Marjut Puputti, Harri Sihto, Jorma Isola, Ralf Butzow, Heikki Joensuu, Nina N. Nupponen
pages 32-38
Abstract | Full Text | Full-Text PDF (241 KB)


Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia
Eulàlia Puigdecanet, Blanca Espinet, Olaya Villa, Lourdes Florensa, Carles Besses, Sergi Serrano, Francesc Solé
pages 39-42
Abstract | Full Text | Full-Text PDF (126 KB)


A molecular study of first and second RB1 mutational hits in retinoblastoma patients
Ana Flávia Belchior de Andrade, Raquel da Hora Barbosa, Fernando Regla Vargas, Sima Ferman, Ana Lúcia Eisenberg, Luisa Fernandes, Cibele R. Bonvicino
pages 43-46
Abstract | Full Text | Full-Text PDF (141 KB)


Myelodysplastic syndromes with isolated deletion of the long arm of the chromosome X as a sole cytogenetic change
Yulia V. Olshanskaya, Alla I. Udovichenko, Lubov A. Vodinskaya, Eugenia N. Glasko, Elena N. Parovitchnikova, Yurii Yu. Lorie, Valentina N. Dvirnik, Valerii G. Savchenko, Elena V. Domracheva
pages 47-50
Abstract | Full Text | Full-Text PDF (103 KB)


Favorable outcome of triploid neuroblastomas: a contribution to the special oncogenesis of neuroblastoma
Ruediger Spitz, David R. Betts, Thorsten Simon, Marc Boensch, Joern Oestreich, Felix K. Niggli, Karen Ernestus, Frank Berthold, Barbara Hero
pages 51-56
Abstract | Full Text | Full-Text PDF (159 KB)


Genome-wide semiquantitative microsatellite analysis of human hepatocellular carcinoma: discrete mapping of smallest region of overlap of recurrent chromosomal gains and losses
Takafumi Nishimura, Naoshi Nishida, Toshiki Komeda, Yoshihiro Fukuda, Iwao Ikai, Yoshio Yamaoka, Kazuwa Nakao
pages 57-65
Abstract | Full Text | Full-Text PDF (437 KB)

Short communications


Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia
Brigitte Royer-Pokora, Detlef Trost, Nicola Müller, Barbara Hildebrandt, Ulrich Germing, Manfred Beier
pages 66-69
Abstract | Full Text | Full-Text PDF (138 KB)


Juvenile myelomonocytic leukemia in a child with Crohn disease
Jeffrey W. Oliver, Brent Farnsworth, Vijay S. Tonk
pages 70-73
Abstract | Full Text | Full-Text PDF (305 KB)


Emergence of chronic myelogenous leukemia in a patient with primary thrombocythemia and absence of BCR/ABL rearrangement
Jesus M. Cesar, Pablo Cabello, Teresa Ferro, J.L. Navarro
pages 74-77
Abstract | Full Text | Full-Text PDF (169 KB)


A diminutive chromosome 21 centromere in acute lymphoblastic leukemia
Kathryn A. Roberts, Mary Martineau, Zoë J. Broadfield, Brenda E.S. Gibson, Louise Harewood, Janet Stewart, Christine J. Harrison
pages 78-81
Abstract | Full Text | Full-Text PDF (1004 KB)


A variant of the SYT-SSX2 fusion gene in a case of synovial sarcoma
Seiji Otsuka, Koichi Nishijo, Tomitaka Nakayama, Tomoki Aoyama, Tatsuya Ishibe, Kotaro R. Shibata, Yasuko Shima, Takashi Nakamura, Takanobu Otsuka, Junya Toguchida
pages 82-88
Abstract | Full Text | Full-Text PDF (352 KB)

Letters to the editor


A suggested protocol for obtaining high-quality skin metaphases from primary cutaneous T-cell lymphoma
Edith Chevret, Martina Prochazkova, Marie Beylot-Barry, Jean-Philippe Merlio
pages 89-91
Full Text | Full-Text PDF (118 KB)


Translocations of 17q21∼qter in neuroblastoma cell lines infrequently include the topoisomerase IIα gene
K. Jin Yoon, Mary K. Danks, Susan T. Ragsdale, Marcus B. Valentine, Virginia A. Valentine
pages 92-94
Full Text | Full-Text PDF (94 KB)

Erratum


Erratum free full text
page 95
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Announcement


Forthcoming events
page 96
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Frontmatter


Table of contents
pages A1-A2
Full-Text PDF (44 KB)

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