Carrier detection and feasibility of prenatal diagnosis of hemophilia B by multiplex polymerase chain reaction
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/BF02592304.pdf
Reference13 articles.
1. Camerino G, Grzeschik KH, Jaye M, De La Salle H, Tolstoshev P, Lecocq J-P, Heillig R, Mandel JL, Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). Proc Natl Acad Sci USA 81:498, 1984
2. Camerino G, Oberle I, Drayna D, Mandel JL, A newMspI restriction fragment length polymorphism in the hemophilia B locus. Hum Genet 71:79, 1985
3. Giannelli F, Factor IX. Baillieres Clin Haematol 2:821, 1989
4. Green PM, Bentley DR, Mibashan RS, Nilsson IM, Giannelli F, Molecular pathology of hemophilia B. EMBO J 8:1067, 1989
5. Hay CW, Robertson KA, Yong SL, Thompson AR, Grove GH, MacGillivray RTA, Use ofBamHI polymorphism in the factor IX gene for the determination of the hemophilia B carrier status. Blood 67:1508, 1986
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1. Indirect diagnosis of haemophilia B by multiplex PCR/RFLP;Clinical and Laboratory Haematology;2005-04
2. Pre- and Perinatal Relations of Hemophilia A and B;Fetal Diagnosis and Therapy;2003
3. Prenatal and molecular diagnosis of hemophilia B;American Journal of Hematology;1996-08
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