Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome (Q34015390)
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English | 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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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome (English)
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D Beysen
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B P Leroy
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A Lucassen
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J R W Yates
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J Clayton-Smith
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H Ilyina
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S Sklower Brooks
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S Christin-Maitre
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M Fellous
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J P Fryns
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J R Kim
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P Lapunzina
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E Lemyre
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F Meire
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L M Messiaen
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C Oley
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M Splitt
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J Thomson
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Y Van de Peer
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R A Veitia
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A De Paepe
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E De Baere
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16 June 2005
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77
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205-218
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