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Further evidence for the location of the blepharophimosis syndrome (BPES) at 3q22.3-q23FRYNS, J. P; STRØMME, P; VAN DEN BERGHE, H et al.Clinical genetics. 1993, Vol 44, Num 3, pp 149-151, issn 0009-9163Article

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)FAN, Jia-Yan; BING HAN; JIE QIAO et al.Mutagenesis. 2011, Vol 26, Num 2, pp 283-289, issn 0267-8357, 7 p.Article

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