Analysis of the two microsatellite repeat polymorphisms of the factor VIII gene in the Turkish population

British Journal of Haematology

Volumn 100, Issue 3, 1998, Pages 589-593

  Jarjanazi, Hamdi ^a   Timur, A Anil ^a   El Maarri, Osman ^a   Çaǧlayan, S Hande ^a  

^a BOGAZICI UNIVERSITY   (Turkey)

Author keywords

Genetic counselling; Haemophilia A; Microsatellite repeat alleles; Multiplex PCR; Turkish population

Indexed keywords

BLOOD CLOTTING FACTOR 8; MICROSATELLITE DNA;

ARTICLE; CHROMOSOME XQ; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; GENETIC COUNSELING; HEMOPHILIA A; HETEROZYGOSITY; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; TURKEY (REPUBLIC);

BASE SEQUENCE; FACTOR VIII; FEMALE; HEMOPHILIA A; HETEROZYGOTE; HUMANS; INTRONS; MALE; MICROSATELLITE REPEATS; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; TURKEY;

EID: 0031865446     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1998.00588.x     Document Type: Article

References (16)

1. Aseev, M., Surin, V., Babodev, K., Gornostaeva, N., Kuznetzova, T., Kascheeva, T., Ivaschenko, T., Solovyev, G., Mikhailov, A., Lebedev. V., Papaian, L., Andreeva, T., Amoashyi, D.M., Vakharlovsky, V. & Baranov, V.S. (1994) Allele frequencies and molecular diagnosis in hemophilia A and B patients from Russia and from some Asian republics of the former U.S.S.R. Prenatal Diagnosis, 14, 513-522.
2. Beidler, J.L., Hilliard, P.R. & Rill, R.L. (1982) Ultrasensitive staining of nucleic acids with silver. Analytical Biochemistry, 126, 374-380.
3. Broker-Vriends, A.H.J.T., Bakker, E., Kanhai, H.H., van Ommen, G.J.B., Reistma, P.H., Van de Kamp, J.J.P. & Briet, E. (1992) The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B. Annals of Hematology, 64, 2-11.
4. Caǧlayan, S.H., Gökmen, Y., Altay, Ç., Aktuǧlu, G., Gürgey, A., Soysal, T., Apak, M., Beksaç, S., Aydmli, K. & Kirdar, B. (1995a) Carrier determination and prenatal diagnosis of hemophilia A by DNA analysis in Turkish families. Turkish Journal of Medical Sciences, 25, 177-182.
5. Caǧlayan, S.H., Gökmen, Y. & Kirdar, B. (1995b) Polymorphisms associated with the FVIII and FIX genes in the Turkish population. Hemophilia, 1, 184-189.
6. Gitschier, J., Wood, W.I., Goralka, T.M., Wion, K.L., Chen, E.Y., Eaton, D.H., Vehar, G.A., Capon, D.J. & Lawn, R.M. (1984) Characterization of the human factor VIII gene. Nature, 312, 326-330.
7. Goodeve, A.C., Tagariello, G., Chuansumrit, A., Preston, F.E. & Peake, I.R. (1996) A rapid and cost effective method for analysis of dinucleotide repeat polymorphisms in the factor VIII gene. Blood Coagulation and Fibrinolysis, 7, 672-677.
8. Green, P.M., Montandon, A.J., Bentley, D.R. & Gianelli, F. (1991) Genetics and molecular biology of hemophilias A and B. Blood Coagulation and Fibrinolysis, 2, 539-565.
9. Hoyer, L.W. (1994) Hemophilia A. New England Journal of Medicine, 330, 38-47.
10. Lalloz, M.R., Schwaab, R., McVey, J.H., Michaelides, K. & Tuddenham, E.G. (1994) Haemophilia A diagnosis by simultaneous analysis of two variable dinucleotide tandem repeats within the factor VIII gene. British Journal of Haematology, 86, 804-809.
11. Lalloz, M.R.A., McVey, J.H., Pattinson, J.H. & Tuddenham, E.G.D. (1991) Haemophilia A diagnosis by analysis of a hypervariable dinucleotide repeat within the factor VIII gene. Lancet, 388, 207-212.
12. Miller, M., Dykes, D.D. & Polesky, H.F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Research, 16, 1215.
13. Peake, I.R., Lillicrap, D.P., Boulyjenkov, V., Briet, E., Chan, V., Ginter, E.R., Kraus, E.M., Ljung, R., Manucci, P.M., Nicloaides, K. & Tuddenham, E.G.D. (1993) Hemophilia: strategies for carrier detection and prenatal diagnosis. Bulletin of the World Health Organization, 77, 429-458.
14. Stoflet, E.S., Koeberl, D.D., Sarkar, G. & Sommer, S.S. (1988) Genomic amplification with transcript sequencing. Science, 239, 491-494.
15. Windsor, S., Taylor, S.A.M. & Lillicrap, D. (1994) Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of haemophilia A. British Journal of Haematology, 86, 810-815.
16. Yip, B., Chan, V. & Chan, T.K. (1994) Intragenic dinucleotide repeats in the factor VIIII gene for the diagnosis of haemophilia A. British Journal of Haematology, 88, 889-891.