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Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Crossref DOI link: https://doi.org/10.1186/s12881-015-0164-3

Published Online: 2015-04-02

Published Print: 2015-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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