Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development-Reference-Cited by-同舟云学术

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

Published:2014-01 Issue:1 Volume:94 Page:23-32
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Peyrard-Janvid Myriam,Leslie Elizabeth J.,Kousa Youssef A.,Smith Tiffany L.,Dunnwald Martine,Magnusson Måns,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.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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