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N. A. Quaderi, S. Schweiger, K. Gaudenz, B. Franco, E. I. Rugarli, W. Berger, G. J. Feldman, M. Volta, G. Andolfi, S. Gilgen-krantz, R. W. Marion, R. C. Hennekam, J. M. Optiz, M. Muenke, H. H. Ropers and A. Ballabio, “Opitz G/BBB Syndrome, a Defect of Midline Development, Is Due to Mutations in a New RING Finger Gene on Xp22,” Nature Genetics, Vol. 17, No. 3, 1997, pp. 285-291. doi:10.1038/ng1197-285

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