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Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

Crossref DOI link: https://doi.org/10.1186/s13039-015-0178-8

Published Online: 2015-09-29

Published Print: 2015-12

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

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