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Dive into the research topics of 'Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations'. Together they form a unique fingerprint.- Sort by
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R. Gruber, G. Rainer, A. Weiss, A. Udvardi, Holger Thiele, Katja Martina Eckl, R. Schupart, Peter Nürnberg, Johannes Zschocke, Matthias Schmuth, B. Volc-platzer, Hans Hennies
Research output: Contribution to journal › Article › peer-review