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The top documents tagged [ocular system]
The sun and our eyes: protection against sunlight
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Apa style guide [compatibility mode]
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A Case of MASS phenotype
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Marfan Syndrome By: Oliver Bell. A mutation or a defect in the gene that makes Fibrillin- 1 (FBN1). Important part of connective tissue. Hereditary (Passed
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Mobile Systems for Chronic Diseases Telemonitoring: Current Status
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Anatomic, Aberrometric , and Biomechanical Characteristics in Patients with Marfan Syndrome
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