Tandem repeats and G-rich sequences are enriched at human CNV breakpoints

PLoS ONE

Volumn 9, Issue 7, 2014, Pages

  Bose, Promita ^a   Hermetz, Karen E ^a   Conneely, Karen N ^a,b   Rudd, M Katharine ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b EMORY UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GUANINE QUADRUPLEX;

ARTICLE; AUTISM; CHILD; CONGENITAL MALFORMATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DEVELOPMENTAL DISORDER; DNA SEQUENCE; G RICH SEQUENCE; GENE LOCUS; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN GENOME; INTELLECTUAL IMPAIRMENT; MAJOR CLINICAL STUDY; NON ALLELIC HOMOLOGOUS RECOMBINATION; PHENOTYPE; SIMULATION; TANDEM REPEAT; TELOMERE; CHROMOSOME FRAGILE SITE; DOUBLE STRANDED DNA BREAK; GENETICS; HUMAN CHROMOSOME; METABOLISM; RECOMBINATION REPAIR;

CHROMOSOME FRAGILE SITES; CHROMOSOMES, HUMAN; DNA BREAKS, DOUBLE-STRANDED; HUMANS; RECOMBINATIONAL DNA REPAIR; TANDEM REPEAT SEQUENCES;

EID: 84903650357     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0101607     Document Type: Article

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