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Dr Andreas Zankl
Centre for Clinical Research
University of Queensland
Australia
Name/email consistency: high
- 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)
- Specific ultrasonographic features of perinatal lethal hypophosphatasia. Zankl, A., Mornet, E., Wong, S. Am. J. Med. Genet. A (2008)
- 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)
