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Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis

✍ Scribed by van Bon, B W M; Koolen, D A; Borgatti, R; Magee, A; Garcia-Minaur, S; Rooms, L; Reardon, W; Zollino, M; Bonaglia, M C; De Gregori, M; Novara, F; Grasso, R; Ciccone, R; van Duyvenvoorde, H A; Aalbers, A M; Guerrini, R; Fazzi, E; Nillesen, W M; McCullough, S; Kant, S G; Marcelis, C L; Pfundt, R; de Leeuw, N; Smeets, D; Sistermans, E A; Wit, J M; Hamel, B C; Brunner, H G; Kooy, F; Zuffardi, O; de Vries, B B A


Book ID
121800895
Publisher
BMJ Publishing Group
Year
2008
Tongue
English
Weight
386 KB
Volume
45
Category
Article
ISSN
0022-2593

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