RECOMBINATION BETWEEN FACTOR VIII:C GENE AND St14 LOCUS
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference8 articles.
1. Genetic mapping and diagnosis of haemophilia A achieved through a Bc1 I polymorphism in the factor VIII gene;Gitchier;Nature,1985
2. A clinically useful DNA probe closely linked to haemophilia A;Harper;Lancet,1984
3. Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe;Oberle;N Engl J Med,1985
4. Carrier testing strategy in haemophilia A;Janco;Lancet,1986
5. Linked and intragenic probes for haemophilia A;Peake;Lancet,1985
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1. Hemophilia A: genetic prediction and linkage studies in all available families in Finland;Clinical Genetics;2008-06-28
2. Polymorphism distribution of Int13, Int22, and St14 VNTRs in a Mexican population and their application in carrier diagnosis of hemophilia A;American Journal of Hematology;2004-08-11
3. Factor VIII gene polymorphisms in the Asian Indian population;Haemophilia;2000-11
4. Studies to detect carriers of haemophilia A in Germanshepherd dogs using diagnostic DNA polymorphisms in the human factor VIII gene;The Veterinary Journal;1997-01
5. Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center;International Journal of Clinical & Laboratory Research;1992-06
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