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

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http://hdl.handle.net/10138/224266

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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

Titel: Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
Författare: Peyrard-Janvid, Myriam; Leslie, Elizabeth J.; Kousa, Youssef A.; Smith, Tiffany L.; Dunnwald, Martine; Magnusson, Mans; Lentz, Brian A.; Unneberg, Per; Fransson, Ingegerd; Koillinen, Hannele K.; Rautio, Jorma; Pegelow, Marie; Karsten, Agneta; Basel-Vanagaite, Lina; Gordon, William; Andersen, Bogi; Svensson, Thomas; Murray, Jeffrey C.; Cornell, Robert A.; Kere, Juha; Schutte, Brian C.
Upphovmannens organisation: Department of Medical and Clinical Genetics
Plastiikkakirurgian yksikkö
Research Programs Unit
Research Programme of Molecular Medicine
Datum: 2014-01-02
Språk: eng
Sidantal: 10
Tillhör serie: American Journal of Human Genetics
ISSN: 0002-9297
DOI: https://doi.org/10.1016/j.ajhg.2013.11.009
Permanenta länken (URI): http://hdl.handle.net/10138/224266
Subject: POPLITEAL PTERYGIUM SYNDROME
CLEFT-PALATE
GRAINY-HEAD
GENOME-WIDE
IRF6
VARIANTS
FAMILIES
DIFFERENTIATION
DROSOPHILA
EMBRYOS
3111 Biomedicine
Referentgranskad: Ja
Licens: cc_by_nc_nd
Användningsbegränsning: openAccess
Parallelpublicerad version: publishedVersion


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