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Short Communication
T-cell acute lymphoblastic leukemia with add(1)(p36) and del(12)(p11) following acute myelocytic leukemia with partial deletion of 9p Chikashi Yoshida, Kazumi Suzukawa, Yukitaka Katsura, Seiichi Shimizu, Harumi Y Mukai, Yuichi Hasegawa, Shigehiko Imagawa, Hiroshi Kojima, Toshiro Nagasawa pages 62-65 Abstract | Full Text | Full-Text PDF (196 KB)
Letter to the Editor
Detection of inv(16)(p13q22) by means of chromosome painting with a 16q-specific probe Ming Li, Yongquan Xue, Yafang Wu, Jinlan Pan pages 86-87 Full Text | Full-Text PDF (152 KB)
A case of adult acute myelocytic leukemia (M5a) with a near-tetraploid karyotype characterized by monosomies 5 and 16 Alessandro Gozzetti, Daniela Tozzuoli, Rosaria Crupi, Maria Teresa Pirrotta, Alessandro Bucalossi, Serena Mazzotta, Francesco Lauria pages 88-89 Full Text | Full-Text PDF (181 KB)
A t(20;21)(q12;q22.3) in a patient with chronic myelocytic leukemia in blastic phase Alessandro Gozzetti, Daniela Tozzuoli, Rosaria Crupi, Sara Gentili, Donatella Raspadori, Alberto Fabbri, Francesco Lauria pages 90-91 Full Text | Full-Text PDF (171 KB)
Detection of micronuclei formation and nuclear anomalies in regenerative nodules of human cirrhotic livers and relationship to hepatocellular carcinoma Terezinha M.B de Almeida, Regina C Leitão, Joyce D Andrade, Willy Beçak, Flair J Carrilho, Shigueko Sonohara pages 16-21 Abstract | Full Text | Full-Text PDF (224 KB)
The occurrence of chromosome segregational defects is an intrinsic and heritable property of oral squamous cell carcinoma cell lines Janet E Reing, Susanne M Gollin, William S Saunders pages 57-61 Abstract | Full Text | Full-Text PDF (566 KB)
Clonal chromosome abnormalities in a plexiform cellular schwannoma Nancy E Joste, Mark I Racz, Karen Dyer Montgomery, Skip Haines, J.David Pitcher pages 73-77 Abstract | Full Text | Full-Text PDF (420 KB)
Trisomy 4 as the sole karyotypic abnormality in a case of acute biphenotypic leukemia with T-lineage markers in minimally differentiated acute myelocytic leukemia Fat-hia Al-Qurashi, Tarek Owaidah, Mohammed A Iqbal, Mahmoud Aljurf pages 66-69 Abstract | Full Text | Full-Text PDF (266 KB)
Detection of t(14;18) in follicular lymphoma by dual-color fluorescence in situ hybridization on paraffin-embedded tissue sections Yosuke Matsumoto, Kenichi Nomura, Sawako Matsumoto, Kyoji Ueda, Mitsushige Nakao, Kazuhiro Nishida, Hideaki Sakabe, Shohei Yokota, Shigeo Horiike, Hirokazu Nakamine, Shigeo Nakamura, Masafumi Taniwaki pages 22-26 Abstract | Full Text | Full-Text PDF (186 KB)
Characterization of large chromosome markers in a malignant fibrous histiocytoma by spectral karyotyping, comparative genomic hybridization (CGH), and array CGH Wen-Hui Weng, Johan Wejde, Jan Åhlén, See-Tong Pang, Weng-Onn Lui, Catharina Larsson pages 27-32 Abstract | Full Text | Full-Text PDF (439 KB)
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma Mattias Höglund, Charlotte Jin, David Gisselsson, Gunnar B Hansen, Felix Mitelman, Fredrik Mertens pages 1-8 Abstract | Full Text | Full-Text PDF (537 KB)
High frequency of genomic instability in Ewing family of tumors Anat Ohali, Smadar Avigad, Ian J Cohen, Isaac Meller, Yehuda Kollender, Josephine Issakov, Yacov Goshen, Isaac Yaniv, Rina Zaizov pages 50-56 Abstract | Full Text | Full-Text PDF (211 KB)
Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma P.S Amare (Kadam), P Ghule, J Jose, M Bamne, P Kurkure, S Banavali, R Sarin, S Advani pages 33-43 Abstract | Full Text | Full-Text PDF (337 KB)
Translocation (11;13)(q23;q14) as the sole abnormality in a childhood de novo acute myelocytic leukemia Kam Sze Tsang, Chi Kong Li, Tai Tap Lau, Angela Pui Yan Wong, Yonna Leung, Margaret Heung Ling Ng pages 78-80 Abstract | Full Text | Full-Text PDF (246 KB)
A fluorescence in situ hybridization study of complex t(9;22) in two chronic myelocytic leukemia cases with a masked Philadelphia chromosome Antonella Zagaria, Luisa Anelli, Francesco Albano, Clelia Tiziana Storlazzi, Arcangelo Liso, Maria Grazia Roberti, Caterina Buquicchio, Vincenzo Liso, Mariano Rocchi, Giorgina Specchia pages 81-85 Abstract | Full Text | Full-Text PDF (257 KB)
Lead article
Wilms tumors develop through two distinct karyotypic pathways Mattias Höglund, David Gisselsson, Gunnar B Hansen, Felix Mitelman pages 9-15 Abstract | Full Text | Full-Text PDF (702 KB)
Editorial Board page CO2 Full-Text PDF (37 KB)
Analysis of human papillomavirus prevalence and TP53 polymorphism in head and neck squamous cell carcinomas Sylvia Sanches Cortezzi, Paola Jocelan Provazzi, João S Sobrinho, José Carlos Mann-Prado, Patrı́cia Maria Pizzo Reis, Suzy Elaine Nobre de Freitas, José Francisco Góis Filho, Érica E Fukuyama, José Antônio Cordeiro, Patrı́cia Maluf Cury, José Vı́tor Maniglia, Luı́sa Lina Villa, Eloiza Helena Tajara, Paula Rahal pages 44-49 Abstract | Full Text | Full-Text PDF (243 KB)
Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences Patricia Canto, Susana Kofman-Alfaro, Ana Luisa Jiménez, Daniela Söderlund, Consuelo Barrón, Edgardo Reyes, Juan Pablo Méndez, Juan Carlos Zenteno pages 70-72 Abstract | Full Text | Full-Text PDF (149 KB)
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