OBO ID: DOID:0060239

Citations

(3 total)

Term: Van der Woude syndrome

Zhang, M., Zhang, J., Zhao, H., Ievlev, V., Zhong, W., Huang, W., Cornell, R.A., Lin, J., Chen, F. (2020) Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family. Frontiers in genetics. 11:562

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. (2014) Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. American journal of human genetics. 94(1):23-32

Ben, J., Jabs, E.W., and Chong, S.S. (2005) Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes. Gene expression patterns : GEP. 5(5):629-638