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[DOI] [PubMed] [Google Scholar] 44.Salomon S., Guignant C., Morel P., Flahaut G., Brault C., Gourguechon C., Fardellone P., Marolleau J.P., Gubler B., Goeb V

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References 1 AbdullahL.EvansJ

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation