FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish

par Balikova, I., Devriendt, K., Fryns, J.-P., Vermeesch, J.R.
Publié 2011

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of publ...

par Menten, B, Maas, N, Thienpont, B, Buysse, K, Vandesompele, J, Melotte, C, de Ravel, T, Van Vooren, S, Balikova, I, Backx, L, Janssens, S, De Paepe, A, De Moor, B, Moreau, Y, Marynen, P, Fryns, J‐P, Mortier, G, Devriendt, K, Speleman, F, Vermeesch, J R
Publié 2006