The molecular basis of hemophilia A in man
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference30 articles.
1. The Metabolic Basis of Inherited Disease;McKee,1983
2. Blood Coagulation
3. Characterization of the human factor VIII gene
4. Molecular cloning of a cDNA encoding human antihaemophilic factor
5. Structure of human factor VIII
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2. A novel deletion of FVIII gene associated with variable levels of FVIII inhibitor*;European Journal of Haematology;2009-04-24
3. Hemophilia A: genetic prediction and linkage studies in all available families in Finland;Clinical Genetics;2008-06-28
4. A Novel PCR—Generated DNA Probe used for Identification of the Most Common Molecular Defects Causing Severe Haemophilia A;Biotechnology & Biotechnological Equipment;2008-01
5. Hemophilia: A Practical Approach to Genetic Testing;Mayo Clinic Proceedings;2005-11
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