Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome

Authors :: Beysen, A.
De Jaegere, S.
Amor, D.
Bouchard, P.
Christin-Maitre, S.
Fellous, M.
Touraine, P.
Grix, A.W.
Hennekam, R.
Meire, F.
Oyen, N.
Wilson, L.C.
Barel, D.
Clayton-Smith, J.
De Ravel, T.
Decock, C.
Delbeke, P.
Ensenauer, R.
Ebinger, F.
Gillessen-Kaesbach, G.
Hendriks, Y.
Kimonis, V.
Laframboise, R.
Laissue, P.
Leppig, K.
Leroy, B.P.
Miller, D.T.
Mowat, D.
Neumann, L.
Plomp, A.S.
Van Regemorter, N.
Wieczorek, D.
Veitia, R.A.
De Paepe, A.
De Baere, E.
Beysen, A.
De Jaegere, S.
Amor, D.
Bouchard, P.
Christin-Maitre, S.
Fellous, M.
Touraine, P.
Grix, A.W.
Hennekam, R.
Meire, F.
Oyen, N.
Wilson, L.C.
Barel, D.
Clayton-Smith, J.
De Ravel, T.
Decock, C.
Delbeke, P.
Ensenauer, R.
Ebinger, F.
Gillessen-Kaesbach, G.
Hendriks, Y.
Kimonis, V.
Laframboise, R.
Laissue, P.
Leppig, K.
Leroy, B.P.
Miller, D.T.
Mowat, D.
Neumann, L.
Plomp, A.S.
Van Regemorter, N.
Wieczorek, D.
Veitia, R.A.
De Paepe, A.
De Baere, E.
Source :: Human Mutation vol.29 (2008) p.E205-E219 [ISSN 1059-7794]
Publication Year :: 2008

Database :: OAIster
Journal :: Human Mutation vol.29 (2008) p.E205-E219 [ISSN 1059-7794]
Notes :: DOI: 10.1002/humu.20819, Human Mutation vol.29 (2008) p.E205-E219 [ISSN 1059-7794], English
Publication Type :: Electronic Resource
Accession number :: edsoai.on1027213482
Document Type :: Electronic Resource

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