A 14q distal chromoanagenesis elucidated by whole genome sequencing
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference28 articles.
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3. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome;Collins;Genome Biol.,2017
4. Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring;de Pagter;Am. J. Hum. Genet.,2015
5. A phenotype map for 14q32.3 terminal deletions;Engels;Am. J. Med. Genet.,2012
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1. Goyal-Naqvi Syndrome (Concurrent Trisomy 10p and Terminal 14q Deletion): A Review of the Literature;Cureus;2021-07-26
2. How Chaotic Is Genome Chaos?;Cancers;2021-03-17
3. The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms;2020-07-17
4. Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis;Cytogenetic and Genome Research;2020
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