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  • Conference proceedings
  • © 1994

Chromosome 12 Aberrations in Human Solid Tumors

Cytogenetics and Molecular Genetics

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Table of contents (17 papers)

  1. Front Matter

    Pages I-XIII
  2. Cytogenetic Background

    1. Front Matter

      Pages 1-1
    2. Specificity and Implications of Chromosome 12 Abnormalities in Pleomorphic Adenomas

      • G. Stenman, J. Bullerdiek, S. Bartnitzke, P. Sahlin, E. Röijer, J. Mark
      Pages 3-15
    3. Involvement of Chromosome 12 in Uterine Leiomyoma

      • R. Vanni, P. Dal Cin
      Pages 16-25
    4. Lipoma Cytogenetics

      • N. Mandahl
      Pages 26-38
    5. Involvement of Chromosome 12 in Well-Differentiated Liposarcoma

      • F. Pedeutour, A. Lamouroux, J. M. Coindre, F. Collin, K. Huffermann, C. Turc-Carel
      Pages 39-45
    6. Breakpoints and Recipient Chromosomes in Pleomorphic Adenomas, Lipomas, and Uterine Leiomyomas — What Do They Tell Us?

      • M. E. Herrmann, G. Belge, C. Stern, P. Dal Cin, J. Bullerdiek, S. Bartnitzke
      Pages 46-51
    7. Trisomy 12 Clusters to Tumors of the Female Genital Tract

      • M. Kiechle-Schwarz, T. Bauknecht, A. Pfleiderer
      Pages 52-55
    8. Cytogenetic and Molecular Studies of Clear-Cell Sarcoma of Tendons and Aponeuroses

      • G. Stenman, P. Sahlin, L. Angervall, P. Meltzer, L.-G. Kindblom
      Pages 61-70
  3. The Molecular Genetics of Chromosome 12

    1. Front Matter

      Pages 71-71
    2. Comparative Gene Mapping: Human Chromosome 12 and Mouse Chromosome 15

      • H. Hameister, C. Klett, G. Hartmann, C. Ebensperger
      Pages 73-78
    3. The Molecular Oncology of 12q13–15

      • B. Rommel, J. Bullerdiek, W. Schloot
      Pages 79-85
  4. Gene Analysis — Methods and Facts

    1. Front Matter

      Pages 87-87
    2. Cell Lines from Tumors Showing 12q13–15 Aberrations

      • B. Kazmierczak, S. Bartnitzke, P. Dal Cin, R. Vanni, J. Bullerdiek
      Pages 89-101
    3. Analysis of DNA from a Specific Chromosome Region

      • N. Ponelies, J. Scheef, M. Köllner, N. Endlich, K. O. Greulich
      Pages 102-123
    4. Chromosome 12 Aberrations in Human Germ Cell Tumors: A Fluorescence In Situ Hybridization Inventory

      • R. F. Suijkerbuijk, R. J. Sinke, L. H. J. Looijenga, B. de Jong, J. W. Oosterhuis, J. J. Cassiman et al.
      Pages 124-137
    5. Development and Characterization of Cell Lines from a Myxoid Liposarcoma with t(12;16)(q13;p11.2) and Trisomy 8

      • F. P. M. Schoenmakers, B. Kazmierczak, P. F. J. Kools, R. Mols, P. Dal Cin, J. Bullerdiek et al.
      Pages 138-150
    6. Analysis of Solid Tumours with Recurrent Breakpoints in Chromosome Region 12q13–15 by Fluorescence In Situ Hybridization Using a Microclone Library

      • P. F. J. Kools, E. F. P. M. Schoenmakers, J. Bullerdiek, U. Claussen, B. Horsthemke, H. Van den Berghe et al.
      Pages 162-172

Editors and Affiliations

  • Zentrum f. Humangenetik u. Genetische Beratung, Universität Bremen, Bremen, Germany

    J. Bullerdiek, S. Bartnitzke

Bibliographic Information

  • Book Title: Chromosome 12 Aberrations in Human Solid Tumors

  • Book Subtitle: Cytogenetics and Molecular Genetics

  • Editors: J. Bullerdiek, S. Bartnitzke

  • DOI: https://doi.org/10.1007/978-3-662-06255-5

  • Publisher: Springer Berlin, Heidelberg

  • eBook Packages: Springer Book Archive

  • Copyright Information: Springer-Verlag Berlin Heidelberg 1994

  • Softcover ISBN: 978-3-662-06257-9Published: 13 July 2013

  • eBook ISBN: 978-3-662-06255-5Published: 17 April 2013

  • Edition Number: 1

  • Number of Pages: XIII, 194

  • Number of Illustrations: 83 b/w illustrations, 14 illustrations in colour

  • Topics: Human Genetics, Pathology, Oncology, Cell Biology

Buy it now

Buying options

eBook USD 84.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access