dc.contributor.author | Grimmel, Mona | |
dc.contributor.author | Sturm, Marc | |
dc.contributor.author | Beck-Wödl, Stefanie | |
dc.contributor.author | Haack, Tobias | |
dc.date.accessioned | 2019-11-11T07:46:46Z | |
dc.date.available | 2019-11-11T07:46:46Z | |
dc.date.issued | 2018 | |
dc.identifier.issn | 1432-1203 | |
dc.identifier.uri | http://hdl.handle.net/10900/94532 | |
dc.language.iso | en | de_DE |
dc.publisher | Springer | de_DE |
dc.relation.uri | http://dx.doi.org/10.1007/s00439-018-1892-1 | de_DE |
dc.subject.ddc | 570 | de_DE |
dc.subject.ddc | 610 | de_DE |
dc.title | De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies | de_DE |
dc.type | Article | de_DE |
utue.quellen.id | 20190321153956_02715 | |
utue.publikation.seiten | 401-411 | de_DE |
utue.personen.roh | Fritzen, Daniel | |
utue.personen.roh | Kuechler, Alma | |
utue.personen.roh | Grimmel, Mona | |
utue.personen.roh | Becker, Jessica | |
utue.personen.roh | Peters, Sophia | |
utue.personen.roh | Sturm, Marc | |
utue.personen.roh | Hundertmark, Hela | |
utue.personen.roh | Schmidt, Axel | |
utue.personen.roh | Kreiss, Martina | |
utue.personen.roh | Strom, Tim M. | |
utue.personen.roh | Wieczorek, Dagmar | |
utue.personen.roh | Haack, Tobias B. | |
utue.personen.roh | Beck-Woedl, Stefanie | |
utue.personen.roh | Cremer, Kirsten | |
utue.personen.roh | Engels, Hartmut | |
dcterms.isPartOf.ZSTitelID | Human Genetics | de_DE |
dcterms.isPartOf.ZS-Issue | 5 | de_DE |
dcterms.isPartOf.ZS-Volume | 137 | de_DE |
utue.fakultaet | 04 Medizinische Fakultät | de_DE |
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