Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
Titel:
Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
Auteur:
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.