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Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation
scientific article
Author/s
author: Feliciano J Ramos, Antonio Musio, Sergey Korolev, Dale Dorsett, Bart L Loeys
Work details
Publication date
January 17, 2007
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Language
English
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