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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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)
    J Clayton-Smith
    S Sklower Brooks
    S Christin-Maitre
    P Lapunzina
    L M Messiaen
    Y Van de Peer

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