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Yi Fen Chang Selected Research

congenital primary Aphakia

5/2022Novel prenatally diagnosed compound heterozygous PXDN variants in fetal congenital primary aphakia and blepharophimosis.

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Yi Fen Chang Research Topics

Disease

1congenital primary Aphakia
05/2022
1Aphakia
05/2022
1Blepharophimosis
05/2022

Drug/Important Bio-Agent (IBA)

15'- O- (9- phenylxanthen- 9- yl)- 2'- deoxynebularineIBA
05/2022

Therapy/Procedure

1Lenses
05/2022