Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome
Author:
Funder
Fundação de Amparo à Pesquisa do Estado de São Paulo
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/article/10.1007/s00439-018-01967-6/fulltext.html
Reference63 articles.
1. Abdollahi MR et al (2009) Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia. Am J Hum Genet 85:737–744. https://doi.org/10.1016/j.ajhg.2009.10.007
2. Bailey JA et al (2002) Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22. Am J Hum Genet 70:83–100. https://doi.org/10.1086/338458
3. Bassett AS, Chow EW (2008) Schizophrenia and 22q11.2 deletion syndrome. Curr Psychiatry Rep 10:148–157
4. Bassett AS, Chow EW, Husted J, Weksberg R, Caluseriu O, Webb GD, Gatzoulis MA (2005) Clinical features of 78 adults with 22q11 Deletion Syndrome. Am J Med Genet A 138:307–313. https://doi.org/10.1002/ajmg.a.30984
5. Bertini V, Azzara A, Legitimo A, Milone R, Battini R, Consolini R, Valetto A (2017) Deletion extents are not the cause of clinical variability in 22q11.2 deletion syndrome: does the interaction between DGCR8 and miRNA-CNVs play a major role? Front Genet 8:47. https://doi.org/10.3389/fgene.2017.00047
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