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Oxford University Press

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Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin–Lowry syndrome

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Complex splicing control of the human Thrombopoietin gene by intronic G runs

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In vivo selection for intronic splicing signals from a randomized pool

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Recent evolutionary acquisition of alternative pre-mRNA splicing and 3′ processing regulations induced by intronic B2 SINE insertion

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