Genetic mapping of the 3MC syndrome: identification of underlying mutations in the lectin complement pathway genes COLEC11 and MASP1 and discovery of a novel paradigm in developmental genetics

Chabchoub, Elyes; Zemni, R.; Kamoun, H.; Mrad, R.; Cogülü, Ö.; Rooryck, C.; Diaz-Font, A.; Osborn, Dp; Hernandez-Hernandez,; Shamseldin, H.; Kenny, J.; Waters, A.; Jenkins, D.; Kaissi, Aa; Leal, Gf; Dallapiccola, B.; Carnevale, F.; Bitner-Glindzicz, M.; Lees, M.; Hennekam, R.; Stanier, P.; Burns, Aj; Alkuraya, Fs; Vermeesch, Joris; Jackmaert, S.; Voet, Thierry; Verloes, A.; Peeters, Hilde; Beals, Pl; Fryns, Jean-Pierre

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Genetic mapping of the 3MC syndrome: identification of underlying mutations in the lectin complement pathway genes COLEC11 and MASP1 and discovery of a novel paradigm in developmental genetics

Proceedings article published in 2012 by Elyes Chabchoub, R. Zemni, H. Kamoun, R. Mrad, Ö. Cogülü, C. Rooryck, A. Diaz-Font, Dp Osborn, Hernandez-Hernandez

, H. Shamseldin, J. Kenny, A. Waters, D. Jenkins, Aa Kaissi, Gf Leal and other authors.

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