Dobrowolski, R., Sasse, P., Schrickel, J. W., Watkins, M., Kim, J., Rackauskas, M., . . . Willecke, K. (2007). The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans.
Stile di citazione ChicagoDobrowolski, Radoslaw, et al. The Conditional Connexin43G138R Mouse Mutant Represents a New Model of Hereditary Oculodentodigital Dysplasia in Humans. 2007.
Citazione MLADobrowolski, Radoslaw, et al. The Conditional Connexin43G138R Mouse Mutant Represents a New Model of Hereditary Oculodentodigital Dysplasia in Humans. 2007.
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