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

Authors :: Barbouti, Aikaterini
Stankiewicz, Pawel
Nusbaum, Chad
Cuomo, Christina
Cook, April
Hoglund, Mattias
Johansson, Bertil
Hagemeijer, Anne
Park, Sung-Sup
Mitelman, Felix
Lupski, James R.
Fioretos, Thoas
Source :: American Journal of Human Genetics. Jan, 2004, Vol. 74 Issue 1, p1, 10 p.
Publication Year :: 2004

Subjects :: Genomes
Tumors
Cloning
Cancer
Chromosomes
Human genetics
Biological sciences

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