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2. Gene conversions are a common cause of von Willebrand disease.

4. Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A( IIC) von Willebrand disease phenotype in an Iranian patient.

5. Effect of DDAVP on nocturnal enuresis in a patient with nephrogenic diabetes insipidus.

6. The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T cell non-Hodgkin lymphoma in a pediatric population.

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