Blepharophimosis, ptosis, epicanthus inversus syndrome, a new case associated with de novo balanced autosomal translocation [46,XY,t(3;7)(q23;q32)]
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference15 articles.
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3. Hereditary Ptosis
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4. Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome;BMC Medical Genetics;2015-09-01
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