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Original articles
Detailed cytogenetic and array analysis of pediatric primitive sarcomas reveals a recurrent CIC–DUX4 fusion gene event Maisa Yoshimoto, Cassandra Graham, Susan Chilton-MacNeill, Eric Lee, Mary Shago, Jeremy Squire, Maria Zielenska, Gino R. Somers pages 1-11 Abstract | Full Text | Full-Text PDF (1725 KB) | Add-Ons
Fusion of EWSR1 with the DUX4 facioscapulohumeral muscular dystrophy region resulting from t(4;22)(q35;q12) in a case of embryonal rhabdomyosarcoma Nicolas Sirvent, Martine Trassard, Nathalie Ebran, Rita Attias, Florence Pedeutour pages 12-18 Abstract | Full Text | Full-Text PDF (887 KB)
Screening of TERC gene amplification as an additional genetic diagnostic test in detection of cervical preneoplastic lesions Nadja Kokalj-Vokač, Tatjana Kodrič, Alenka Erjavec-Škerget, Andreja Zagorac, Iztok Takač pages 19-22 Abstract | Full Text | Full-Text PDF (124 KB)
Telomere aggregates in trisomy 21 amniocytes Efrat Hadi, Reuven Sharony, Lilach Goldberg-Bittman, Tal Biron-Shental, Moshe Fejgin, Aliza Amiel pages 23-26 Abstract | Full Text | Full-Text PDF (111 KB)
Telomere aggregate formation in placenta specimens of pregnancies complicated with pre-eclampsia Rivka Sukenik-Halevy, Moshe Fejgin, Devora Kidron, Lilach Goldberg-Bittman, Reuven Sharony, Tal Biron-Shental, Yona Kitay-Cohen, Aliza Amiel pages 27-30 Abstract | Full Text | Full-Text PDF (148 KB)
TP53 R72P and MDM2 SNP309 polymorphisms in modification of childhood acute lymphoblastic leukemia susceptibility Thuy N. Do, Esma Ucisik-Akkaya, Charronne F. Davis, Brittany A. Morrison, M. Tevfik Dorak pages 31-36 Abstract | Full Text | Full-Text PDF (119 KB)
Detection of chromosomal abnormalities associated with chronic lymphocytic leukemia: what is the best method? Maha el-Taweel, Carole Barin, Florence Cymbalista, Virginie Eclache pages 37-42 Abstract | Full Text | Full-Text PDF (106 KB)
Polymorphisms in one-carbon metabolism pathway genes and risk for bladder cancer in a Tunisian population Kamel Rouissi, Slah Ouerhani, Elisabete Oliveira, Raja Marrakchi, Lotfi Cherni, Fethi Ben Othman, Mohamed R. Ben Slama, Mohamed Sfaxi, Mohsen Ayed, Mohamed Chebil, António Amorim, Maria João Prata, Amel Benammar Elgaaied pages 43-53 Abstract | Full Text | Full-Text PDF (135 KB)
Novel SYT–SSX fusion transcript variants in synovial sarcoma Euthimios Dimitriadis, Demetra Rontogianni, Anastasios Kyriazoglou, Anna Takou, Kostantina Frangia, Nikolaos Pandis, Theoni Trangas pages 54-58 Abstract | Full Text | Full-Text PDF (607 KB)
Homozygous deletion of CDKN2A (p16, p14) and CDKN2B (p15) genes is a poor prognostic factor in adult but not in childhood B-lineage acute lymphoblastic leukemia: a comparative deletion and hypermethylation study Miyoung Kim, Seon-Hee Yim, Nam-Sun Cho, Seong-Ho Kang, Dae-Hyun Ko, Bora Oh, Tae Young Kim, Hyun Jung Min, Cha Ja She, Hyoung Jin Kang, Hee Yung Shin, Hyo-Sup Ahn, Sung Soo Yoon, Byoung Kook Kim, Hai-Rim Shin, Kyu Sup Han, Han Ik Cho, Dong Soon Lee pages 59-65 Abstract | Full Text | Full-Text PDF (357 KB)
HMGA2–NFIB fusion in a pediatric intramuscular lipoma: a novel case of NFIB alteration in a large deep-seated adipocytic tumor Anne Pierron, Carla Fernandez, Esma Saada, Frédérique Keslair, Géraldine Hery, Hélène Zattara, Florence Pedeutour pages 66-70 Abstract | Full Text | Full-Text PDF (552 KB)
Short communications
Cytogenetic, fluorescence in situ hybridization, and molecular characterization of chronic myeloid leukemia in chronic phase with four BCR/ABL1 fusion signals: a case report Maria Teresa Vargas, Maria Angeles Portero, Alicia Rodríguez, Juana Reyes, Carmen Fernández-Novoa pages 71-74 Abstract | Full Text | Full-Text PDF (373 KB)
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast–ovarian cancer syndromes: a case report Laura Papi, Domenico Palli, Laura Masi, Anna Laura Putignano, Caterina Congregati, Ines Zanna, Francesca Marini, Francesca Giusti, Ettore Luzi, Francesco Tonelli, Maurizio Genuardi, Maria Luisa Brandi, Alberto Falchetti pages 75-79 Abstract | Full Text | Full-Text PDF (123 KB)
Cytogenetic study of a pulmonary sclerosing hemangioma María J. Pareja, María T. Vargas, Ana Sánchez, José Ibáñez, Ricardo González-Cámpora pages 80-84 Abstract | Full Text | Full-Text PDF (1362 KB)
Establishment and conventional cytogenetic characterization of three gastric cancer cell lines Mariana Ferreira Leal, José Luiz Martins do Nascimento, Carla Elvira Araújo da Silva, Maria Fernanda Vita Lamarão, Danielle Queiroz Calcagno, André Salim Khayat, Paulo Pimentel Assumpção, Isabel Rosa Cabral, Marília de Arruda Cardoso Smith, Rommel Rodríguez Burbano pages 85-91 Abstract | Full Text | Full-Text PDF (725 KB)
Letters to the editor
FGFR3 amplification in the absence of IGH@–FGFR3 fusion t(4;14) in myeloma Fabiola Quintero-Rivera, Riem El-Sabbagh Badr, P. Nagesh Rao pages 92-93 Full Text | Full-Text PDF (127 KB)
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia Tae Sung Park, Sang-Guk Lee, Jaewoo Song, Kyung-A Lee, Juwon Kim, Jong Rak Choi, Seung Tae Lee, Rolf Marschalek, Claus Meyer pages 94-95 Full Text | Full-Text PDF (320 KB)
Frontmatter
Table of Contents pages A1-A2 Full-Text PDF (44 KB)
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