Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

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 journalArticlepeer-review

318 Scopus citations

Fingerprint

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.

Medicine & Life Sciences