Results 101 to 110 of about 3,916 (200)

Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene [PDF]

open access: yes, 2018
Balogh, István   +7 more
core  

Utilization of an automated machine learning approach for the detection of granular corneal dystrophy via slit lamp photographs. [PDF]

open access: yesBMC Ophthalmol
Yavari N   +18 more
europepmc   +1 more source

CRISPR Base Editing Correction of TGFBI Mutations in Autosomal Dominant Corneal Dystrophies. [PDF]

open access: yesInvest Ophthalmol Vis Sci
Chen J   +10 more
europepmc   +1 more source

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