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

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Publication year
1997
Author(s)
Quaderi, N.A.
Schweiger, S.
Gaudenz, K.
Franco, B.
Rugarli, E.I.
Berger, W.
Feldman, G.J.
Volta, M.
Andolfi, G.
Gilgenkrantz, S.
Marion, R.W.
Hennekam, R.C.M.
Opitz, J.M.
Muenke, M.
Ropers, H.H.
Ballabio, A.
Source
Nature Genetics, 17, 3, (1997), pp. 285-291
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/24575   https://hdl.handle.net/2066/24575
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