Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/82005
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dc.contributor.authorGecz, J.-
dc.contributor.authorHaan, E.-
dc.date.issued2012-
dc.identifier.citationThe Lancet, 2012; 380(9854):1630-1631-
dc.identifier.issn0140-6736-
dc.identifier.issn1474-547X-
dc.identifier.urihttp://hdl.handle.net/2440/82005-
dc.description.statementofresponsibilityJozef Gecz, Eric Haan-
dc.language.isoen-
dc.publisherElsevier-
dc.rightsCopyright © 2012 Elsevier Ltd. All rights reserved.-
dc.subjectHumans-
dc.subjectMutation-
dc.subjectFemale-
dc.subjectMale-
dc.subjectIntellectual Disability-
dc.subjectExome-
dc.titleNew mutations and sporadic intellectual disability-
dc.typeJournal article-
dc.identifier.doi10.1016/S0140-6736(12)61603-1-
pubs.publication-statusPublished-
dc.identifier.orcidGecz, J. [0000-0002-7884-6861]-
dc.identifier.orcidHaan, E. [0000-0002-7310-5124]-
Appears in Collections:Aurora harvest
Paediatrics publications

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