Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends

Human Mutation

Volumn 22, Issue 3, 2003, Pages 245-251

  Chuzhanova, Nadia ^a,b   Abeysinghe, Shaun S ^a   Krawczak, Michael ^c   Cooper, David N ^a  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b SOBOLEV INSTITUTE OF MATHEMATICS   (Russian Federation)

^c UNIVERSITY OF KIEL   (Germany)

Author keywords

Breakpoint junction sequences; Cancer; Complexity analysis; Database; Deletion; Gene rearrangement; Inherited disease; Mutational mechanisms; Recombination, homologous; Recombination, nonhomologous; Translocation

Indexed keywords

DNA; LYMPHOCYTE ANTIGEN RECEPTOR; SINGLE STRANDED DNA;

ARTICLE; CHROMOSOME TRANSLOCATION; DNA FLANKING REGION; GENE DELETION; GENE INSERTION; GENE MUTATION; GENE REARRANGEMENT; GENETIC DATABASE; HUMAN; HUMAN GENOME; INVERTED REPEAT; MALIGNANT NEOPLASTIC DISEASE; MUTATIONAL ANALYSIS; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; PROTEIN SECONDARY STRUCTURE;

3' FLANKING REGION; 5' FLANKING REGION; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; DATABASES, GENETIC; DNA; DNA, NEOPLASM; GENES, T-CELL RECEPTOR ALPHA; GENETIC DISEASES, INBORN; GENOME, HUMAN; HUMANS; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; IMMUNOGLOBULIN HEAVY CHAINS; INTERNET; MODELS, GENETIC; NEOPLASMS; NUCLEIC ACID CONFORMATION; RECEPTORS, LDL; REPETITIVE SEQUENCES, NUCLEIC ACID; RETINOBLASTOMA PROTEIN; TRANSLOCATION, GENETIC;

EID: 0041761326     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10253     Document Type: Article

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