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Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements.
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A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains.
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4
Unbalanced translocations arise from diverse mutational mechanisms including chromothripsis.
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6
Mechanisms for Complex Chromosomal Insertions.
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8
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
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A rare example of germ-line chromothripsis resulting in large genomic imbalance.
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Chromosomal Instability and Chromoanagenesis as Forces for Genomic Evolution.
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Sperm DNA Fragmentation as a Marker of Chromoanagenesis Occurrence During Spermatogenesis.
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Multifocal Genomic Reconstruction Leading to Germline Structural Variants.
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Origin and Fate of Micronuclei on the Road to Chromoanagenesis.
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Chromoanagenesis in Multiple Myeloma: A Comprehensive Overview.
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Structural and Mechanistic Diversity of Constitutional Chromoanagenesis.
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ISCN and Chromoanagenesis.
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Identification and Characterization of Chromothripsis by Optical Genome Mapping.
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本文引用的文献

2
Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients.
Blood. 2011 Jul 21;118(3):675-8. doi: 10.1182/blood-2011-03-344069. Epub 2011 May 31.
4
Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.
Hum Mol Genet. 2011 May 15;20(10):1975-88. doi: 10.1093/hmg/ddr078. Epub 2011 Feb 25.
5
Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline.
Hum Mol Genet. 2011 May 15;20(10):1916-24. doi: 10.1093/hmg/ddr073. Epub 2011 Feb 24.
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Break-induced replication is highly inaccurate.
PLoS Biol. 2011 Feb 15;9(2):e1000594. doi: 10.1371/journal.pbio.1000594.
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New mutations and intellectual function.
Nat Genet. 2010 Dec;42(12):1036-8. doi: 10.1038/ng1210-1036.
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Detection of clinically relevant exonic copy-number changes by array CGH.
Hum Mutat. 2010 Dec;31(12):1326-42. doi: 10.1002/humu.21360. Epub 2010 Nov 2.

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