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Proceedings of the National Academy of Sciences of the United States of America|March 21, 2007
The implications of alternative splicing in the ENCODE protein complementMichael L Tress, Pier Luigi Martelli, Adam Frankish, et al.Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.Pageof 2