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Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family.
BMC Ophthalmol
; 23(1): 446, 2023 Nov 07.
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en Inglés
| MEDLINE | ID: mdl-37932670
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