Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome
Titel:
Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome
Auteur:
Beysen, D. Raes, J. Leroy, B.P. Lucassen, A. Yates, J.R.W. Clayton-Smith, J. Ilyina, H. Brooks, S. Sklower Christin-Maitre, S. Fellous, M. Fryns, J.P. Kim, J.R. Lapunzina, P. Lemyre, E. Meire, F. Messiaen, L.M. Oley, C. Splitt, M. Thomson, J. Peer, Y. Van de Veitia, R.A. De Paepe, A. De Baere, E.