Publication:
Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study

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dc.bibliographiccitation.firstpage1216
dc.bibliographiccitation.issue4
dc.bibliographiccitation.journalAmerican Journal of Medical Genetics Part A
dc.bibliographiccitation.lastpage1221
dc.bibliographiccitation.volume185
dc.contributor.authorGangfuß, Andrea
dc.contributor.authorYigit, Gökhan
dc.contributor.authorAltmüller, Janine
dc.contributor.authorNürnberg, Peter
dc.contributor.authorCzeschik, Johanna Christina
dc.contributor.authorWollnik, Bernd
dc.contributor.authorBögershausen, Nina
dc.contributor.authorBurfeind, Peter
dc.contributor.authorWieczorek, Dagmar
dc.contributor.authorKaiser, Frank
dc.contributor.authorRoos, Andreas
dc.contributor.authorKölbel, Heike
dc.contributor.authorSchara‐Schmidt, Ulrike
dc.contributor.authorKuechler, Alma
dc.date.accessioned2021-04-14T08:30:46Z
dc.date.available2021-04-14T08:30:46Z
dc.date.issued2021
dc.identifier.doi10.1002/ajmg.a.62070
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/83369
dc.language.isoen
dc.notes.internDOI Import GROB-399
dc.relation.eissn1552-4833
dc.relation.issn1552-4825
dc.titleIntellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study
dc.typejournal_article
dc.type.internalPublicationyes
dspace.entity.typePublication

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