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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome |
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| Authors: | 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 Van de Peer Y Veitia R A De Paepe A De Baere E |
| Affiliation: | Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium. |
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| 本文献已被 ScienceDirect PubMed 等数据库收录！ | |