HAEMOPHILIA A: TWO RECOMBINATIONS DETECTED WITH PROBE Stl4
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference7 articles.
1. Carner testing strategy in haemophilia A;Janco;Lancet,1986
2. A clinically useful DNA probe closely linked to haemophilia A;Harper;Lancet,1984
3. X-chromosome-specific probe DX13 for carrier detection and first trimester prenatal diagnosis in haemophilia A;To̸nnesen;Lancet,1984
4. First trimester prenatal diagnosis and detection of carriers of haemophilia A using the linked DNA probe DX13;Winter;Br Med J,1985
5. Linked and intragenic probes for haemophilia A;Peake;Lancet,1985
Cited by 13 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. Hemophilia A: genetic prediction and linkage studies in all available families in Finland;Clinical Genetics;2008-06-28
2. X-Chromosome inactivation in the Wiskott-Aldrich syndrome: A marker for detection of the carrier state and identfication of cell lineages expressing the gene defect;Genomics;1989-01
3. 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
4. First trimester prenatal diagnosis of haemophilia A: Two years' experience;Prenatal Diagnosis;1988-07
5. Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese;Human Genetics;1988-06
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