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Dive into the research topics of 'Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22'. Together they form a unique fingerprint.- Sort by
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Nandita A. Quaderi, Susann Schweiger, Karin Gaudenz, Brunella Franco, Elena I. Rugarli, Wolfgang Berger, George J. Feldman, Manuela Volta, Grazia Andolfi, S. Gilgenkrantz, Robert W. Marion, Raoul C.M. Hennekam, John M. Opitz, Maximilian Muenke, H. Hilger Ropers, Andrea Ballabio
Research output: Contribution to journal › Article › peer-review