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Dental Phenotype in Jalili Syndrome Due to a c.1312 dupC Homozygous Mutation in the CNNM4 Gene

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Dental Phenotype in Jalili Syndrome Due to a c.1312 dupC Homozygous Mutation in the CNNM4 Gene

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In Vivo Retinal Pigment Epithelium Imaging using Transscleral Optical Imaging in Healthy Eyes

Ophthalmic system and method for clinical device using transcleral illumination with multiple points source

Three-dimensional imaging of integrated circuits with macro- to nanoscale zoom

Compositions and methods for delivering nucleic acids to cochlear and vestibular cells

Calcium phosphate formation on titanium-based surfaces: bioactivity evaluated by in vitro methods

Design and validation of a foldable and photovoltaic wide-field epiretinal prosthesis

Mutations in the polyglutamylase geneTTLL5, expressed in photoreceptor cells and spermatozoa, are associated with cone-rod degeneration and reduced male fertility

In-situ photopolymerization and monitoring device for controlled shaping of tissue fillers, replacements or implants

Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract

Strontium hydroxyapatite and strontium carbonate as templates for the precipitation of calcium-phosphates in the absence and presence of fluoride