Restriction fragment length polymorphisms of the CYP11B1 gene in the Japanese population
نویسندگان
چکیده
منابع مشابه
The Frequencies of three Factor IX-Linked Restriction Fragment Length Polymorphisms in Iranian Patients with Hemophilia B
Background: Hemophilia B is an X-linked recessive coagulation disorder caused by factor IX deficiency. Analysis of factor IX gene polymorphisms is considered the best approach for prenatal diagnosis and carrier detection of hemophilia B where the identification of gene mutation is not easily possible. Objective: To study the frequency of three factor IX-linked restriction fragment length polym...
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ژورنال
عنوان ژورنال: Japanese journal of human genetics
سال: 1993
ISSN: 0021-5074
DOI: 10.1007/bf01883711