Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome von Wieland, I, Weidner, C, Ciccone, R, Lapi, E, McDonald-McGinn, D, Kress, W, Jakubiczka, S, Collmann, H, Zuffardi, O, Zackai, E, Wieacker, P

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