"Diagnosis of Hemophilia B Carriers, Using Taq I and Xmn I Polymorphisms of the FactorIX Gene in Iranian Individuals"
Hemophilia B is factor IX deficiency and is inherited as X-linked recessive disorder. The subject of carrier detection in hemophilias has received new impetus in the last several years. Analysis of factor IX gene polymorphisms is considered the best approach for prenatal diagnosis and hemophilia B c...
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| Main Authors: | , , , |
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| Format: | Book |
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Tehran University of Medical Sciences,
2003-09-01T00:00:00Z.
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