Recombinant DNA methods in hemophilia A: carrier detection and prenatal diagnosis.

doi:10.1055/s-2007-1002687

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Article

Recombinant DNA methods in hemophilia A: carrier detection and prenatal diagnosis.

Seminars in thrombosis and hemostasis - 1 Oct 1990

Sadler J E

Abstract excerpt

Hemophilia A is a serious inherited bleeding disorder of man that is caused by deficiency of blood coagulation Factor VIII. Major clinical problems in the treatment of hemophilia A include the transmission of disease by therapeutic blood products and the development of alloantibody inhibitors to...

Topics

DNA, Recombinant
Factor VIII
Genetic Carrier Screening
Hemophilia A
Humans
Mutation
Pedigree
Prenatal Diagnosis

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