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

American Journal of Human Genetics

Volumn 74, Issue 1, 2004, Pages 1-10

  Barbouti, Aikaterini ^a   Stankiewicz, Pawel ^b   Nusbaum, Chad ^d   Cuomo, Christina ^d   Cook, April ^d   Höglund, Mattias ^a   Johansson, Bertil ^a   Hagemeijer, Anne ^e   Park, Sung Sup ^b,f   Mitelman, Felix ^a   Lupski, James R ^b,c   Fioretos, Thoas ^a  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c TEXAS CHILDREN S HOSPITAL   (United States)

^d WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^e UNIVERSITY OF LEUVEN   (Belgium)

^f Seoul National University Hospital   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

PALINDROMIC DNA;

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 17Q; CHROMOSOME NOR; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CLUSTER ANALYSIS; FEMALE; GENE MAPPING; GENE STRUCTURE; GENOME; HEMATOLOGIC MALIGNANCY; HUMAN; HYPOTHESIS; ISOCHROMOSOME; MALE; NEOPLASM; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 9144264835     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/380648     Document Type: Article

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