Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndrome

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.
Source :: American Journal of Human Genetics. August, 2005, Vol. 77 Issue 2, p205, 14 p.
Publication Year :: 2005

Subjects :: Human genetics -- Research
Genetic disorders -- Research
Chromosome abnormalities -- Research
Biological sciences

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