Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

Show simple item record

dc.contributor.author Peyrard-Janvid, Myriam
dc.contributor.author Leslie, Elizabeth J.
dc.contributor.author Kousa, Youssef A.
dc.contributor.author Smith, Tiffany L.
dc.contributor.author Dunnwald, Martine
dc.contributor.author Magnusson, Mans
dc.contributor.author Lentz, Brian A.
dc.contributor.author Unneberg, Per
dc.contributor.author Fransson, Ingegerd
dc.contributor.author Koillinen, Hannele K.
dc.contributor.author Rautio, Jorma
dc.contributor.author Pegelow, Marie
dc.contributor.author Karsten, Agneta
dc.contributor.author Basel-Vanagaite, Lina
dc.contributor.author Gordon, William
dc.contributor.author Andersen, Bogi
dc.contributor.author Svensson, Thomas
dc.contributor.author Murray, Jeffrey C.
dc.contributor.author Cornell, Robert A.
dc.contributor.author Kere, Juha
dc.contributor.author Schutte, Brian C.
dc.date.accessioned 2017-09-18T10:51:01Z
dc.date.available 2017-09-18T10:51:01Z
dc.date.issued 2014-01-02
dc.identifier.citation Peyrard-Janvid , M , Leslie , E J , Kousa , Y A , Smith , T L , Dunnwald , M , Magnusson , M , Lentz , B A , Unneberg , P , Fransson , I , Koillinen , H K , Rautio , J , Pegelow , M , Karsten , A , Basel-Vanagaite , L , Gordon , W , Andersen , B , Svensson , T , Murray , J C , Cornell , R A , Kere , J & Schutte , B C 2014 , ' Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development ' , American Journal of Human Genetics , vol. 94 , no. 1 , pp. 23-32 . https://doi.org/10.1016/j.ajhg.2013.11.009
dc.identifier.other PURE: 35640296
dc.identifier.other PURE UUID: 30520ae9-55c2-44fb-b7bd-6cf98a2f2bbc
dc.identifier.other WOS: 000329888400003
dc.identifier.other Scopus: 84891832380
dc.identifier.uri http://hdl.handle.net/10138/224266
dc.format.extent 10
dc.language.iso eng
dc.relation.ispartof American Journal of Human Genetics
dc.rights cc_by_nc_nd
dc.rights.uri info:eu-repo/semantics/openAccess
dc.subject POPLITEAL PTERYGIUM SYNDROME
dc.subject CLEFT-PALATE
dc.subject GRAINY-HEAD
dc.subject GENOME-WIDE
dc.subject IRF6
dc.subject VARIANTS
dc.subject FAMILIES
dc.subject DIFFERENTIATION
dc.subject DROSOPHILA
dc.subject EMBRYOS
dc.subject 3111 Biomedicine
dc.title Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development en
dc.type Article
dc.contributor.organization Department of Medical and Clinical Genetics
dc.contributor.organization Plastiikkakirurgian yksikkö
dc.contributor.organization Research Programs Unit
dc.contributor.organization Research Programme of Molecular Medicine
dc.description.reviewstatus Peer reviewed
dc.relation.doi https://doi.org/10.1016/j.ajhg.2013.11.009
dc.relation.issn 0002-9297
dc.rights.accesslevel openAccess
dc.type.version publishedVersion

Files in this item

Total number of downloads: Loading...

Files Size Format View
1_s2.0_S0002929713005247_main.pdf 3.474Mb PDF View/Open

This item appears in the following Collection(s)

Show simple item record