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Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1–q24.2 contiguous gene deletion

dc.contributor.authorSeeley, Andrea H.en_US
dc.contributor.authorDurham, Mark A.en_US
dc.contributor.authorMicale, Mark A.en_US
dc.contributor.authorWesolowski, Jeffreyen_US
dc.contributor.authorFoerster, Bradley R.en_US
dc.contributor.authorMartin, Donna M.en_US
dc.date.accessioned2014-08-06T16:49:51Z
dc.date.availableWITHHELD_13_MONTHSen_US
dc.date.available2014-08-06T16:49:51Z
dc.date.issued2014-08en_US
dc.identifier.citationSeeley, Andrea H.; Durham, Mark A.; Micale, Mark A.; Wesolowski, Jeffrey; Foerster, Bradley R.; Martin, Donna M. (2014). "Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1–q24.2 contiguous gene deletion." American Journal of Medical Genetics Part A 164(8): 2062-2068.en_US
dc.identifier.issn1552-4825en_US
dc.identifier.issn1552-4833en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/108054
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.otherJPH3en_US
dc.subject.otherSLC7A5en_US
dc.subject.otherDeletion Syndromeen_US
dc.subject.otherFBXO31en_US
dc.subject.otherMacrocerebellumen_US
dc.subject.otherMAP1LC3Ben_US
dc.titleMacrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1–q24.2 contiguous gene deletionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/108054/1/ajmga36569.pdf
dc.identifier.doi10.1002/ajmg.a.36569en_US
dc.identifier.sourceAmerican Journal of Medical Genetics Part Aen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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