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Dominant mutations in GRHL3 cause Van der Woude syndrome and disrupt oral periderm development
Myriam Peyrard-Janvid*, Elizabeth J. Leslie, Youssef A. Kousa, Tiffany L. Smith, Martine Dunnwald, Måns Magnusson, Brian A. Lentz, Per Unneberg, Ingegerd Fransson, Hannele K. Koillinen, Jorma Rautio, Marie Pegelow, Agneta Karsten, Lina Basel-Vanagaite, William Gordon, Bogi Andersen, Thomas Svensson, Jeffrey C. Murray, Robert A. Cornell, Juha Kere
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
178
Scopus
citations