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Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, 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 BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: laissue p. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388 Free article.
BMP15 and premature ovarian failure: causal mutations, variants, polymorphisms?
Lakhal B, Laissue P, Braham R, Elghezal H, Saâd A, Fellous M, Veitia RA. Lakhal B, et al. Among authors: laissue p. Clin Endocrinol (Oxf). 2010 Mar;72(3):425-6. doi: 10.1111/j.1365-2265.2009.03651.x. Epub 2009 Jun 8. Clin Endocrinol (Oxf). 2010. PMID: 19508678 No abstract available.
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