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Thromb Haemost 1992; 68(05): 622-623
DOI: 10.1055/s-0038-1646330
DOI: 10.1055/s-0038-1646330
Letter to the Editor
Usefulness of Determination of Factor VIII Intron 7 Polymorphism by a Non-Radioactive Technique for Carrier Detection of Hemophilia A
Further Information
Publication History
Received 07 April 1992
Accepted after revision 22 June 1992
Publication Date:
04 July 2018 (online)
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REFERENCES
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- 2 Kogan SC, Gitschier J. Genetic prediction of hemophilia A. In: PCR Protocols: A Guide to Methods and Applications. Innis MA, Gelfand DH, Sninsky JJ, White TJ. (eds) Academic Press, San Diego, CA: 1990. pp 288-299
- 3 Gitschier J, Drayna D, Tuddenham EGD, White RL, Lawn RM. Genetic mapping and diagnosis of hemophilia A achieved through a Bcll polymorphism in the factor VIII gene. Nature 1985; 314: 738-740
- 4 Lalloz MRA, McVey JH, Pattinson JK, Tuddenham EGD. Hemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene. Lancet 1991; 338: 207-211
- 5 Hendy JG, Cauchi MN. Direct detection of β thalassemic mutations: use of biotin-labelled allele specific probes. Am J Hematol 1990; 34: 151-153