Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2 , in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome | Journal of Human Genetics

Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2 , in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome | Journal of Human Genetics

Heterozygous 17-bp deletion in the forkhead transcription factor gene, FOXL2, in a Japanese family with blepharophimosis-ptosis-epicanthus inversus syndrome

• T. Yamada, 
• S. Hayasaka, 
• M. Matsumoto, 
• Budu, 
• T. Esa, 
• Y. Hayasaka & 
• M. Endo 

Journal of Human Genetics volume 46, pages733–736(2001)Cite this article

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