Detection of carriers of haemophilia A: use of bioassays and restriction fragment length polymorphisms (RFLP)
Author:
Publisher
Wiley
Subject
Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1445-5994.1996.tb00884.x/fullpdf
Reference36 articles.
1. Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis;Peake;Blood Coagulation and Fibrinolysis,1993
2. Prenatal diagnosis of hemophilia involving grandpaternal mosaicism;Lebo;Am J Med Genet,1993
3. Detection of haemophilia carriers: multivariate analysis compared with discriminant analysis using up to five factor VIII variates;Duncan;Br J Haematol,1984
4. Carrier detection in hemophilia A: A cooperative international study. II The efficacy of a universal discriminant;Green;Blood,1986
5. Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition;Tuddenham;Nucleic Acids Res,1994
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Clinical Application of Factor VIII:C to VWF:Ag Ratio for the Screening of Haemophilia A Carriers;Journal of Clinical Medicine;2022-03-18
2. Grandpaternal mosaicism in a family with isolated haemophilia A;British Journal of Haematology;1999-12
3. Carrier detection in haemophilia A families: comparison of conventional coagulation parameters with DNA polymorphism analysis - first report from India;Haemophilia;1999-07
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