U-type exchange is the most frequent mechanism for inverted duplication with terminal deletion rearrangements

Journal of Medical Genetics

Volumn 46, Issue 10, 2009, Pages 694-702

  Rowe, L R ^a   Lee, J Y ^b   Rector, L ^a   Kaminsky, E B ^b   Brothman, A R ^a,c   Martin, C L ^b   South, S T ^a,c  

^a ARUP INSTITUTE FOR CLINICAL AND EXPERIMENTAL PATHOLOGY   (United States)

^b EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMATID EXCHANGE; CHROMOSOME 10Q; CHROMOSOME 13Q; CHROMOSOME 15Q; CHROMOSOME 18P; CHROMOSOME 18Q; CHROMOSOME 22Q; CHROMOSOME 2Q; CHROMOSOME 4P; CHROMOSOME 5P; CHROMOSOME 6Q; CHROMOSOME 8; CHROMOSOME 8P; CHROMOSOME ANALYSIS; CHROMOSOME ARM; CHROMOSOME BREAKAGE; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; DICENTRIC CHROMOSOME; HUMAN; IN SITU HYBRIDIZATION; INVERTED REPEAT; MEIOSIS; PARENT; PRIORITY JOURNAL; SISTER CHROMATID;

CHROMOSOME BANDING; CHROMOSOMES, HUMAN; COMPARATIVE GENOMIC HYBRIDIZATION; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; SISTER CHROMATID EXCHANGE;

EID: 70349656642     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2008.065052     Document Type: Article

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