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

M. Muenke

Department of Pediatrics

University of Pennsylvania




Name/email consistency: high



  • Department of Pediatrics, University of Pennsylvania, Philadelphia, USA. 1997


  1. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Muenke, M., Gripp, K.W., McDonald-McGinn, D.M., Gaudenz, K., Whitaker, L.A., Bartlett, S.P., Markowitz, R.I., Robin, N.H., Nwokoro, N., Mulvihill, J.J., Losken, H.W., Mulliken, J.B., Guttmacher, A.E., Wilroy, R.S., Clarke, L.A., Hollway, G., Adès, L.C., Haan, E.A., Mulley, J.C., Cohen, M.M., Bellus, G.A., Francomano, C.A., Moloney, D.M., Wall, S.A., Wilkie, A.O. Am. J. Hum. Genet. (1997) [Pubmed]
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