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Original article
Molecular cytogenetic analysis of clustered sporadic and familial renal cell carcinoma-associated 3q13∼q22 breakpoints Daniëlle Bodmer, Irene Janssen, Yvonne Jonkers, Eva van den Berg, Trijnie Dijkhuizen, Maria Debiec-Rychter, Eric Schoenmakers, Ad Geurts van Kessel pages 95-100 Abstract | Full Text | Full-Text PDF (186 KB)
Fluorescence in situ hybridization for the study of cell lineage involvement in myelodysplastic syndromes with chromosome 5 anomalies Kristina Anderson, Ingrid Arvidsson, Björn Jacobsson, Robert Hast pages 101-107 Abstract | Full Text | Full-Text PDF (258 KB)
Banded chromosomes versus fluorescence in situ hybridization in the diagnosis of mantle cell lymphoma: a lesson from three cases Anwar N Mohamed, Wassim Ali, Fred Kopptich, Ayad al Katib pages 108-112 Abstract | Full Text | Full-Text PDF (129 KB)
Losses in chromosomes 17, 19, and 22q in neurofibromatosis type 1 and sporadic neurofibromas: a comparative genomic hybridization analysis Takamasa Koga, Hiroshi Iwasaki, Masako Ishiguro, Akio Matsuzaki, Masahiro Kikuchi pages 113-120 Abstract | Full Text | Full-Text PDF (293 KB)
Comparative genomic hybridization detects specific cytogenetic abnormalities in pediatric ependymomas and choroid plexus papillomas Jacques Grill, Hervé Avet-Loiseau, Arielle Lellouch-Tubiana, Nicolas Sévenet, Marie-José Terrier-Lacombe, Anne-Marie Vénuat, François Doz, Christian Sainte-Rose, Chantal Kalifa, Gilles Vassal pages 121-125 Abstract | Full Text | Full-Text PDF (70 KB)
Spontaneous clinical and cytogenetic remission of aplastic anemia in a patient with del(13q) Takashi Saitoh, Minoru Saiki, Takao Kumagai, Yoshimasa Kura, Umihiko Sawada, Takashi Horie pages 126-128 Abstract | Full Text | Full-Text PDF (82 KB)
High resolution analysis of chromosome 18 alterations in ulcerative colitis-related colorectal cancer Jonathan P Terdiman, Daniela E Aust, Cornell G Chang, Robert F Willenbucher, Gustavo B Baretton, Frederic M Waldman pages 129-137 Abstract | Full Text | Full-Text PDF (1188 KB)
Transient myeloproliferative disorder in a phenotypically normal infant with i(21q) mosaicism Shi-Qi Wu, Kwan Tien Loh, Xiao-Rong Chen, Wan Jong Joo, Leo Mascarenhas pages 138-140 Abstract | Full Text | Full-Text PDF (296 KB)
Short communication
Molecular cytogenetic characterization of a complex rearrangement involving chromosomes 9 and 22 in a case of Ph-negative chronic myeloid leukemia Clelia Tiziana Storlazzi, Luisa Anelli, Cecilia Surace, Angelo Lonoce, Antonella Zagaria, Mauro Nanni, Paola Curzi, Mariano Rocchi pages 141-145 Abstract | Full Text | Full-Text PDF (217 KB)
Precursor T-lymphoblastic leukemia with a novel t(1;22)(p34;q13) K.F Wong, C.C So, G Lau pages 146-148 Abstract | Full Text | Full-Text PDF (106 KB)
Letter to the editor
The BCR/ABL-extra signal fluorescence in situ hybridization system reliably detects deletions upstream of the ABL locus: implications for reporting of results and followup of chronic myelogenous leukemia patients Christel Müller, Evelin Hennig, Christina Franke, Rainer Krahl, Sabine Leiblein, Dietger Niederwieser, Michael W.N Deininger pages 149-150 Full Text | Full-Text PDF (50 KB)
Mutations in the runt homology domain of CBFα2 in myeloid malignancies with acquired trisomy 21 Jennifer Snaddon, Michael Neat, Jude Fitzgibbon, Matthew L Smith, Ama Z Rohatiner, T.Andrew Lister, John A Amess pages 151-152 Full Text | Full-Text PDF (51 KB)
Myelodysplastic syndrome with transformation to AML-M7 in a 46,XX male patient Lai-Ching Lau, Ping Lim, Weng-Onn Lui, Yap-Yee Chong pages 153-154 Full Text | Full-Text PDF (49 KB)
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