Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/82005
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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Gecz, J. | - |
dc.contributor.author | Haan, E. | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | The Lancet, 2012; 380(9854):1630-1631 | - |
dc.identifier.issn | 0140-6736 | - |
dc.identifier.issn | 1474-547X | - |
dc.identifier.uri | http://hdl.handle.net/2440/82005 | - |
dc.description.statementofresponsibility | Jozef Gecz, Eric Haan | - |
dc.language.iso | en | - |
dc.publisher | Elsevier | - |
dc.rights | Copyright © 2012 Elsevier Ltd. All rights reserved. | - |
dc.source.uri | http://dx.doi.org/10.1016/s0140-6736(12)61603-1 | - |
dc.subject | Humans | - |
dc.subject | Mutation | - |
dc.subject | Female | - |
dc.subject | Male | - |
dc.subject | Intellectual Disability | - |
dc.subject | Exome | - |
dc.title | New mutations and sporadic intellectual disability | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1016/S0140-6736(12)61603-1 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Gecz, J. [0000-0002-7884-6861] | - |
dc.identifier.orcid | Haan, E. [0000-0002-7310-5124] | - |
Appears in Collections: | Aurora harvest Paediatrics publications |
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