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Publications by Lokman Balyen
Clinical Features of a Pediatric Case With Cone Dystrophy
Van Medical Journal
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A Case of Idiopathic Perifoveal Telangiectasia Preceded by Features of Cone Dystrophy
Eye
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Arts
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Ophthalmology
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Cone Dystrophy in Patient With HomozygousRP1L1Mutation
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Homozygosity Mapping in Patients With Cone–Rod Dystrophy: Novel Mutations and Clinical Characterizations
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
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Hereditary Crystalline Stromal Dystrophy of Schnyder. I. Clinical Features of a Family With Hyperlipoproteinaemia.
British Journal of Ophthalmology
Molecular Neuroscience
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Cone Beam Computed Tomography Features of Cherubism: A Case Report
International Journal of Medical and Dental Case Reports
Clinical Course of Cone Dystrophy Caused by Mutations in the RPGR Gene
Graefe's Archive for Clinical and Experimental Ophthalmology
Molecular Neuroscience
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Sensory Systems
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Ophthalmic Features of Cone-Rod Dystrophy Caused by Pathogenic Variants in the ALMS1 Gene
Acta Ophthalmologica
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Pediatric Psoriasis: Clinical Features and Course
Open Access Journal of Biomedical Science
Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.
British Journal of Ophthalmology
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