Two different forms of palindrome resolution in the human genome: Deletion or translocation

Human Molecular Genetics

Volumn 17, Issue 8, 2008, Pages 1184-1191

  Kato, Takema ^a   Inagaki, Hidehito ^a   Kogo, Hiroshi ^a   Ohye, Tamae ^a   Yamada, Kouji ^a   Emanuel, Beverly S ^b,c   Kurahashi, Hiroki ^a  

^a FUJITA HEALTH UNIVERSITY   (Japan)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PALINDROMIC DNA;

ARTICLE; AT RICH SEQUENCE; BASE PAIRING; DNA POLYMORPHISM; DNA REPAIR; DNA SEQUENCE; GENE DELETION; GENE FREQUENCY; GENE IDENTIFICATION; GENE INSERTION; GENE REARRANGEMENT; GENE REPLICATION; GENE TRANSLOCATION; GENETIC VARIABILITY; GENOMIC INSTABILITY; HUMAN; HUMAN EXPERIMENT; NORMAL HUMAN; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY;

AT RICH SEQUENCE; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; GENE DELETION; GENOMIC INSTABILITY; HUMANS; MUTAGENESIS, INSERTIONAL; NUCLEIC ACID CONFORMATION; REPETITIVE SEQUENCES, NUCLEIC ACID; TRANSLOCATION, GENETIC; VARIATION (GENETICS);

EUKARYOTA; PROKARYOTA;

EID: 41849149326     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddn008     Document Type: Article

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