Fold-back mechanism originating inv-dup-del rearrangements in chromosomes 13 and 15
Author:
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
https://link.springer.com/content/pdf/10.1007/s10577-023-09720-0.pdf
Reference36 articles.
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2. Ballarati L et al (2007) 13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients. J Med Genet 44(1):1–6. https://doi.org/10.1136/jmg.2006.043059
3. Burssed B et al (2022) Mechanisms of structural chromosomal rearrangement formation. Mol Cytogenet 15(1):1–15. https://doi.org/10.1186/s13039-022-00600-6
4. Carvalho CMB, Lupski JR (2016) Mechanisms underlying structural variant formation in genomic disorders. Nat Rev Genet 17(4):224–238. https://doi.org/10.1038/nrg.2015.25
5. Cowan CA et al (2004) Ephrin-B2 reverse signaling is required for axon pathfinding and cardiac valve formation but not early vascular development. Dev Biol 271(2):263–271. https://doi.org/10.1016/j.ydbio.2004.03.026
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1. Identification of small-sized intrachromosomal segments at the ends of INV–DUP–DEL patterns;Journal of Human Genetics;2023-07-10
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