Search Results - Schmidt, G.

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    Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma by Scholz, Christian (Author) , Golas, M. M. (Author) , Weber, R. G. (Author) , Hartmann, C. (Author) , Lehmann, U. (Author) , Sahm, Felix (Author) , Schmidt, G. (Author) , Auber, B. (Author) , Sturm, M. (Author) , Schlegelberger, B. (Author) , Illig, T. (Author) , Steinemann, D. (Author) , Hofmann, W. (Author) ,


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    ATC-Code / Hrsg.: Wissenschaftliches Institut der AOK (WIdO) / 1999 by Fricke, Uwe (Author) , Lemmer, Björn (Author) , Günther, J. (Author) , Lohse, M. (Author) , Mengel, K. (Author) , Schmidt, G. (Author) , Scholz, H. (Author) ,


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    Standards der Behandlung und Begutachtung von Transsexuellen der Deutschen Gesellschaft für Sexualforschung, der Akademie für Sexualmedizin und der Gesellschaft für Sexual Wisse... by Becker, Sophinette (Author) , Bosinski, H.A.G. (Author) , Clement, Ulrich (Author) , Sicher, W. (Author) , Goerlich, T. (Author) , Hartmann, U. (Author) , Kockott, Götz (Author) , Langer, D. (Author) , Preuss, W. (Author) , Schmidt, G. (Author) , Springer, A. (Author) , Wille, R. (Author) ,


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