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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Wolfram Kress

Department of Human Genetics

University of Würzburg



Name/email consistency: high



  • Department of Human Genetics, University of Würzburg, Germany. 2000 - 2006


  1. 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) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
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