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Dive into the research topics of 'The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans'. Together they form a unique fingerprint.- Sort by
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Radoslaw Dobrowolski, Philipp Sasse, Jan W. Schrickel, Marcus Watkins, Jung Sun Kim, Mindaugas Rackauskas, Clemens Troatz, Alexander Ghanem, Klaus Tiemann, Joachim Degen, Feliksas F. Bukauskas, Roberto Civitelli, Thorsten Lewalter, Bernd K. Fleischmann, Klaus Willecke
Research output: Contribution to journal › Article › peer-review