Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

查看全文 作　　者：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;R.A.;Veitia;A.;D