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

Fourth European Cytogenetics Conference, Date: 2003/09/06 - 2003/09/09, Location: Bologna, Italy

Publication date: 2003-01-01

Volume: 46 Pages: 333 -

Publisher: Elsevier Science

Annales de Génétique

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:

Barbouti, A

Stankiewicz, P ; Nussbaum, C ; Birren, B ; Höglund, M ; Johansson, B ; Hagemeijer-Hausman, Anne ; Park, SS ; Mitelman, F ; Lupski, JR ; Fioretos, T

Keywords:

Genetics & Heredity