Dominant hereditary optic atrophy with bitemporal field defects.
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Disease↗
Biomedical subjects
Publications and source records attributed to F P CALHOUN.
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Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.