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

著者: Nandita Quaderi, Susann Schweiger, Karin Gaudenz, Brunella Franco, Elena I. Rugarli, Wolfgang Berger, George Feldman, Manuela Volta, Grazia Andolfi, S Gilgenkrantz, Robert W. Marion, Raoul C. M. Hennekam, John M. Opitz, Maximilian Muenke, Hilger H. Ropers, Andrea Ballabio - Nature Genetics 1997 被引用: 370