LINKED AND INTRAGENIC PROBES FOR HAEMOPHILIA A
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference9 articles.
1. Prenatal diagnosis of haemophilia A by factor VIII gene analysis;Antonarakis;Lancet,1985
2. Factor VIII gene specific probe for prenatal diagnosis of haemophilia A;Din;Lancet,1985
3. X-chromosome specific probe DX13 for carrier detection and prenatal diagnosis is haemophilia A;Tonnenson;Lancet,1984
4. Antenatal diagnosis and carrier detection of haemophilia A using a factory VIII gene probe;Gitschier;Lancet,1985
5. A clinically useful DNA probe closely linked to haemophilia A;Harper;Lancet,1984
Cited by 11 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. Multiplex analysis of two intragenic microsatellite repeat polymorphisms in the genetic diagnosis of haemophilia A;British Journal of Haematology;1994-04
2. Hemophilia A;Hematology/Oncology Clinics of North America;1992-10
3. The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B;Annals of Hematology;1992-01
4. The Molecular Pathology of Hemophilia A;Transfusion Medicine Reviews;1991-07
5. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms;British Journal of Haematology;1988-09
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