Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome
Open Access
- 1 December 2001
- journal article
- case report
- Published by Springer Nature in Journal of Human Genetics
- Vol. 46 (12) , 733-736
- https://doi.org/10.1007/s100380170009
Abstract
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