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

Erwin Petek

Institute of Medical Biology and Human Genetics

University of Graz



Name/email consistency: high



  • Institute of Medical Biology and Human Genetics, University of Graz, Austria. 2000 - 2003


  1. Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus. Petek, E., Windpassinger, C., Mach, M., Rauter, L., Scherer, S.W., Wagner, K., Kroisel, P.M. Am. J. Med. Genet. A (2003) [Pubmed]
  2. Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. Petek, E., Windpassinger, C., Simma, B., Mueller, T., Wagner, K., Kroisel, P.M. J. Hum. Genet. (2003) [Pubmed]
  3. Characterization of a de novo partial trisomy 22q13-qter in a patient by microFISH. Petek, E., Köstl, G., Mutz, I., Wagner, K., Kroisel, P.M. Clin. Dysmorphol. (2000) [Pubmed]
  4. Localization of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescencein situ hybridisation. Petek, E., Windpassinger, C., Egger, H., Kroisel, P.M., Wagner, K. Cytogenet. Cell Genet. (2000) [Pubmed]
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