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

Dr Andreas Zankl

Centre for Clinical Research

University of Queensland



Name/email consistency: high



  • Genetic Health Queensland, Royal Children's Hospital, Brisbane, Australia. 2008
  • CHUV, Lausanne, Switzerland. 2007


  1. Prenatal and postnatal presentation of severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN) due to the FGFR3 Lys650Met mutation. Zankl, A., Elakis, G., Susman, R.D., Inglis, G., Gardener, G., Buckley, M.F., Roscioli, T. Am. J. Med. Genet. A (2008) [Pubmed]
  2. Specific ultrasonographic features of perinatal lethal hypophosphatasia. Zankl, A., Mornet, E., Wong, S. Am. J. Med. Genet. A (2008) [Pubmed]
  3. Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome. Zankl, A., Pachman, L., Poznanski, A., Bonafé, L., Wang, F., Shusterman, Y., Fishman, D.A., Superti-Furga, A. J. Bone Miner. Res. (2007) [Pubmed]
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