Genes, Chromosomes and Cancer

Cover image for Vol. 53 Issue 6

June 2014

Volume 53, Issue 6

Pages 447–536

  1. Research Articles

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    2. Research Articles
    1. You have free access to this content
      Frequent translocations of 11q13.2 and 19p13.2 in ovarian cancer (pages 447–453)

      Liang Wang, Antonia Wenners, Felix Hilpert, Regina Fredrik, Francesca Micci, Wiebke Onkes, Amke Caliebe, Nicolai Maass, Jörg Weimer and Norbert Arnold

      Article first published online: 24 FEB 2014 | DOI: 10.1002/gcc.22152

    2. The effect of UGT1A and UGT2B polymorphisms on colorectal cancer risk: Haplotype associations and gene–environment interactions (pages 454–466)

      Andrea Y. Angstadt, Terryl J. Hartman, Samuel M. Lesko, Joshua E. Muscat, Junjia Zhu, Carla J. Gallagher and Philip Lazarus

      Article first published online: 12 FEB 2014 | DOI: 10.1002/gcc.22157

    3. Complex IGH rearrangements in multiple myeloma: Frequent detection discrepancies among three different probe sets (pages 467–474)

      Gina Y. Kim, Ana Gabrea, Yulia N. Demchenko, Leif Bergsagel, Anna V. Roschke and W. Michael Kuehl

      Article first published online: 3 MAR 2014 | DOI: 10.1002/gcc.22158

    4. Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material (pages 475–486)

      Francois Le Loarer, Lei Zhang, Christopher D. Fletcher, Agnes Ribeiro, Samuel Singer, Antoine Italiano, Agnes Neuville, Aurélie Houlier, Frederic Chibon, Jean-Michel Coindre and Cristina R. Antonescu

      Article first published online: 3 MAR 2014 | DOI: 10.1002/gcc.22159

    5. Increased frequency of minimal homozygous deletions is associated with poor prognosis in primary malignant melanoma patients (pages 487–496)

      Sebastiana Boi, Toma Tebaldi, Angela Re, Chiara Cantaloni, Valentina Adami, Mattia Barbareschi, Mario Cristofolini, Luigi Pasini and Alessandro Quattrone

      Article first published online: 24 FEB 2014 | DOI: 10.1002/gcc.22160

    6. Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma (pages 516–523)

      Anna Wójcicka, Małgorzata Czetwertyńska, Michał Świerniak, Joanna Długosińska, Monika Maciąg, Agnieszka Czajka, Kinga Dymecka, Anna Kubiak, Adam Kot, Rafał Płoski, Albert de la Chapelle and Krystian Jażdżewski

      Article first published online: 6 MAR 2014 | DOI: 10.1002/gcc.22162

    7. Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93% (pages 524–536)

      Verena Mühlbacher, Melanie Zenger, Susanne Schnittger, Sandra Weissmann, Franziska Kunze, Alexander Kohlmann, Frauke Bellos, Wolfgang Kern, Torsten Haferlach and Claudia Haferlach

      Article first published online: 11 MAR 2014 | DOI: 10.1002/gcc.22163