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Fourteen new cases contribute to the characterization of th..:
Van der Aa, Nathalie
;
Rooms, Liesbeth
;
Vandeweyer, Geert
...
European Journal of Medical Genetics. 52 (2009) 2-3 - p. 94-100 , 2009
Link:
https://doi.org/10.1016/j.ejmg.2009.02.006
RT Journal T1
Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2009.02.006&Exemplar=1&LAN=DE A1 Van der Aa, Nathalie A1 Rooms, Liesbeth A1 Vandeweyer, Geert A1 van den Ende, Jenneke A1 Reyniers, Edwin A1 Fichera, Marco A1 Romano, Corrado A1 Delle Chiaie, Barbara A1 Mortier, Geert A1 Menten, Björn A1 Destrée, Anne A1 Maystadt, Isabelle A1 Männik, Katrin A1 Kurg, Ants A1 Reimand, Tiia A1 McMullan, Dom A1 Oley, Christine A1 Brueton, Louise A1 Bongers, Ernie M.H.F. A1 van Bon, Bregje W.M. A1 Pfund, Rolph A1 Jacquemont, Sebastien A1 Ferrarini, Alessandra A1 Martinet, Danielle A1 Schrander-Stumpel, Connie A1 Stegmann, Alexander P.A. A1 Frints, Suzanna G.M. A1 de Vries, Bert B.A. A1 Ceulemans, Berten A1 Kooy, R. Frank PB Elsevier BV YR 2009 SN 1769-7212 JF European Journal of Medical Genetics VO 52 IS 2-3 SP 94 OP 100 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2009.02.006 DO https://doi.org/10.1016/j.ejmg.2009.02.006 SF ELIB - SuUB Bremen
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