FIGURE SUMMARY
Title

Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development

Authors
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., and Schutte, B.C.
Source
Full text @ Am. J. Hum. Genet.

ZFIN is incorporating published figure images and captions as part of an ongoing project. Figures from some publications have not yet been curated, or are not available for display because of copyright restrictions.

EXPRESSION / LABELING:
Gene:
Fish:
Anatomical Term:
Stage: Shield
Acknowledgments