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• W2344103441 abstract "Discovery of genetic alterations that cause human birth defects provide key opportunities to improve the diagnosis, treatment, and family counseling. Frequently, however, these opportunities are limited by the lack of knowledge about the normal functions of the affected genes. In many cases, there is more information about the gene's orthologs in model organisms, including Drosophila melanogaster . Despite almost a billion years of evolutionary divergence, over three‐quarters of genes linked to human diseases have Drosophila homologs. With a short generation time, a twenty‐fold smaller genome, and unique genetic tools, the conserved functions of genes are often more easily elucidated in Drosophila than in other organisms. Here we present how this applies to Cornelia de Lange syndrome, as a model for how Drosophila can be used to increase understanding of genetic syndromes caused by mutations with broad effects on gene transcription and exploited to develop novel therapies. © 2016 Wiley Periodicals, Inc." @default.
• W2344103441 created "2016-06-24" @default.
• W2344103441 creator A5071795589 @default.
• W2344103441 date "2016-04-20" @default.
• W2344103441 modified "2023-10-14" @default.
• W2344103441 title "The<i>Drosophila melanogaster</i>model for Cornelia de Lange syndrome: Implications for etiology and therapeutics" @default.
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• W2344103441 doi "https://doi.org/10.1002/ajmg.c.31490" @default.
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