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Behçet's syndrome: a family study and the elucidation of a genetic role.
  1. L Berman,
  2. B Trappler,
  3. T Jenkins


    A family with features of the mucocutaneous ocular syndrome is described. A 4-generation study reveals that the condition has been inherited as an autosomal dominant trait with variable expressivity. Psychiatric symptoms and myalgia have been prominent features peculiar to our patients.

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