| disease | Q12136 |
| eye disease | Q3041498 |
| hereditary disorder | Q3311537 |
| P1995 | health specialty | ophthalmology | Q161437 |
| Q76598698 | AV SYNDROMES AND CONGENITAL OPHTHALMOPLEGIA |
| Q46250842 | Adaptive optics imaging of inherited retinal diseases. |
| Q73784587 | Advising patients with hereditary eye disease |
| Q76646751 | CONGENITAL OPHTHALMOPLEGIA AND MUSCULAR FIBROSIS |
| Q35532323 | Cataract surgery in megalocornea; report of case of two extractions and review of cases since 1931 |
| Q77800008 | Current DNA-based tests for hereditary eye disease |
| Q30860642 | DATA CONCERNING THE PSEUDOGLAUCOMA |
| Q75761153 | Dystrophia reticularis laminae pigmentosae retinae, an earlier not described hereditary eye disease |
| Q76716133 | ELECTROMYOGRAPHIC ASPECTS OF CONGENITAL OPHTHALMOPLEGIA |
| Q54401746 | Editorial: Hereditary eye disease and prenatal diagnosis. |
| Q26752831 | Genetic manipulation for inherited neurodegenerative diseases: myth or reality? |
| Q76968377 | HEREDITARY EYE DISEASES WITH SPECIAL REFERENCE TO RETINITIS PIGMENTOSA |
| Q93838015 | Hereditary Eye Disease in Tasmania |
| Q57106148 | Lamina cribrosa excavation syndrome--pseudoglaucoma |
| Q39423311 | Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions |
| Q54223399 | MEGALOCORNEA AND INFANTILE GLAUCOMA |
| Q78359581 | MEGALOCORNEA IN CONGENITAL GLAUCOMA |
| Q76942391 | MEGALOCORNEA: REPORT OF A CASE WITH THE SIGNS OF PIGMENTARY GLAUCOMA |
| Q78833135 | Megalocornea and its relation to congenital glaucoma |
| Q54103947 | Molecular exploration of the R91W (RPE65 gene) in Tunisian patients with early onset retinal dystrophy and early onset retinitis pigmentosa |
| Q35539873 | Ophthalmic genetics/inherited eye disease |
| Q51272512 | PSEUDOTUMOR CEREBRI. REPORT OF SIX CASES COMPARED WITH ONE CASE OF PSEUDOPAPILLEDEMA |
| Q78791196 | Relation of megalocornea to congenital glaucoma according to gonioscopic findings |
| Q92163635 | Retinal miRNA Functions in Health and Disease |
| Q44673700 | Snowflake vitreoretinal degeneration: follow-up of the original family |
| Q26748615 | Surgical and molecular pathology of pancreatic neoplasms |
| Q76799766 | THE FLORIFORM CATARACT |
| Q50982540 | THE SYNDROME OF BLUE SCLERAE WITH KERATOGLOBUS |
| Q78416973 | ULTRASONICS DIAGNOSIS OF MICROPHTHALMIA WITHOUT MICROCORNEA, WITH MACROPHAKIA, HIGH HYPERMETROPIA ASSOCIATED WITH TAPETO-RETINAL DEGENERATION, A GLAUCOMATOUS PREDISPOSITION AND DENTAL ANOMALIES (NEW FAMILIAL SYNDROME) |
Search more.