Analysis of the AluI polymorphism in intron 1 of the human coagulation factor VIII gene: A new marker for the hemophilia a carrier detection
Author:
Publisher
Pleiades Publishing Ltd
Subject
Genetics
Link
http://link.springer.com/content/pdf/10.1134/S1022795407040151.pdf
Reference22 articles.
1. Gitschier, J., Wood, W.I., Goralka, T.M., et al., Characterization of the Human Factor VIII Gene, Nature, 1984, vol. 312, pp. 326–330.
2. Lakich, D., Kazazian, H.H., Antonarakis, S.E., et al., Inversions Disrupting the Factor VIII Gene Are a Common Cause of Severe Haemophilia A, Nat. Genet., 1993, vol. 5, pp. 236–241.
3. Naylor, J., Brinke, A., Hassock, S., et al., Characteristic mRNA Abnormality Found in Half the Patients with Severe Haemophilia A Is Due to Large DNA Inversions, Hum. Mol. Genet., 1993, vol. 2, pp. 1773–1778.
4. Bagnall, R.D., Waseem, N., Green, P.M., et al., Recurrent Inversion Breaking Intron 1 of the Factor VIII Gene Is a Frequent Cause of Severe Hemophilia A, Blood, 2002, vol. 99, pp. 168–174.
5. Lalloz, M.R., McVey, J.H., Pattinson, J.K., et al., Haemophilia A Diagnosis by Analysis of a Hypervariable Dinucleotide Repeat within the Factor VIII Gene, Lancet, 1991, vol. 338, pp. 207–211.
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