Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias. Autor Le Goff, C, Mahaut, C, Wang, L, Allali, S, Abhyankar, A, Jensen, S, Zylberberg, L, Collod-Beroud, G, Bonnet, D, Alanay, Y, Brady, A, Cordier, M, Devriendt, K, Genevieve, D, Kiper, P, Kitoh, H, Krakow, D, Lynch, SA, Le Merrer, M, Mégarbane, A, Mortier, G, Odent, S, Polak, M, Rohrbach, M, Sillence, D