Wolfram Kress
Department of Human Genetics
University of Würzburg
Germany
Name/email consistency: high
- Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. Kress, W., Schropp, C., Lieb, G., Petersen, B., Büsse-Ratzka, M., Kunz, J., Reinhart, E., Schäfer, W.D., Sold, J., Hoppe, F., Pahnke, J., Trusen, A., Sörensen, N., Krauss, J., Collmann, H. Eur. J. Hum. Genet. (2006)
- Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses). Kress, W., Collmann, H., Büsse, M., Halliger-Keller, B., Mueller, C.R. Cytogenet. Cell Genet. (2000)
- An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly. Kress, W., Petersen, B., Collmann, H., Grimm, T. Cytogenet. Cell Genet. (2000)