Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream ofFOXL2as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome


D. Beysen,J. Raes,B.P. Leroy,A. Lucassen,J.R.W. Yates,J. Clayton-Smith,H. Ilyina,S. Sklower Brooks,S. Christin-Maitre,M. Fellous,J.P. Fryns,J.R. Kim,P. Lapunzina,E. Lemyre,F. Meire,L.M. Messiaen,C. Oley,M. Splitt,J. Thomson,Y. Van de Peer, et al.


The American Journal of Human Genetics




August 2005

Copyright © 2005, Elsevier

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