The constitutional t(11;22): Implications for a novel mechanism responsible for gross chromosomal rearrangements

Clinical Genetics

Volumn 78, Issue 4, 2010, Pages 299-309

  Kurahashi, H ^a   Inagaki, H ^a   Ohye, T ^a   Kogo, H ^a   Tsutsumi, M ^a   Kato, T ^a   Tong, M ^a   Emanuel, B S ^b,c  

^a FUJITA HEALTH UNIVERSITY   (Japan)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Cruciform; Gross chromosomal rearrangements; Non B DNA; Palindrome; Translocation

Indexed keywords

PALINDROMIC DNA; SINGLE STRANDED DNA;

AT RICH REPEAT; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 22; DNA POLYMORPHISM; DNA REPLICATION; DNA STRUCTURE; DOUBLE STRANDED DNA BREAK; GENOMIC INSTABILITY; HUMAN; PRIORITY JOURNAL; REVIEW; SPERMATOGENESIS;

AT RICH SEQUENCE; CHROMOSOME ABERRATIONS; CHROMOSOME BREAKPOINTS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; DNA, CRUCIFORM; DNA, SINGLE-STRANDED; FEMALE; GENOME, HUMAN; GENOMIC INSTABILITY; HUMANS; MALE; REPETITIVE SEQUENCES, NUCLEIC ACID; SPERMATOGENESIS; TRANSLOCATION, GENETIC;

ROBERTSONIA;

EID: 77956406859     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2010.01445.x     Document Type: Review

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