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The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.

Author:
  • Aikaterini Barbouti
  • Pawel Stankiewicz
  • Chad Nusbaum
  • Christina Cuomo
  • April Cook
  • Mattias Höglund
  • Bertil Johansson
  • Anne Hagemeijer
  • Sung-Sup Park
  • Felix Mitelman
  • James R Lupski
  • Thoas Fioretos
Publishing year: 2004
Language: English
Pages: 1-10
Publication/Series: American Journal of Human Genetics
Volume: 74
Issue: 1
Document type: Journal article
Publisher: Cell Press

Keywords

  • Medical Genetics

Other

Published
  • ISSN: 0002-9297
Thoas Fioretos
E-mail: thoas [dot] fioretos [at] med [dot] lu [dot] se

Principal investigator

Translational Genomic and Functional Studies of Leucemia

+46 46 222 45 95

+46 70 334 33 67

BMC C13

66

Professor

Division of Clinical Genetics

+46 46 222 45 95

+46 70 334 33 67

BMC C13

66

Professor

Translational Genomic and Functional Studies of Leucemia

+46 46 222 45 95

+46 70 334 33 67

BMC C13

66