Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Biochemistry
Link
http://link.springer.com/content/pdf/10.1007/BF02591668.pdf
Reference30 articles.
1. Ahrens P, Kruse TA, Schwartz M, Rasmussen PB, Din N, A newHindIII restriction fragment length polymorphism in the hemophilia A locus. Hum Genet 76:127, 1987
2. Antonarakis SE, Waber PG, Kuttur SD, Patel AS, Kazazian HH, Mellis MA, Pittman DD, Wozney JM, Toole JJ, Hemophilia A: detection of molecular defects and of carriers by DNA analysis. N Engl J Med 313:842, 1985
3. Antonarakis SE, Youssoufian H, Kazazian HH, Molecular genetics of hemophilia A in man. Mol Biol Med 4:81, 1987
4. Driscoll MC, Miller CH, Goldberg JD, Aledort LM, Hoyer LW, Golbus M, Recombination between factor VIII: C gene and St14 locus. Lancet II:279, 1986
5. Duncan BM, Tunbridge LJ, Duncan EM, Lloyd JV, Detection of haemophilia carriers: multivariate analysis compared with discriminant analysis using up to five factor VIII variates. Br J Haematol 57:113, 1984
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