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Haemophilia
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- ... blood clot. Mutations in the F8 gene cause hemophilia A, the most common form of this bleeding disorder. ... The most common mutation in people with severe hemophilia A is a rearrangement of genetic material called an ...
- ... NCBI Gene ClinVar Bolton-Maggs PH, Pasi KJ. Haemophilias A and B. Lancet. 2003 May 24;361( ... 03)13405-8. Citation on PubMed Bowen DJ. Haemophilia A and haemophilia B: molecular insights. Mol Pathol. ...
- ... Diagnosis and treatment of inherited factor X deficiency. Haemophilia. 2008 Nov;14(6):1176-82. doi: 10. ... immunological assays even in the molecular biology era. Haemophilia. 2011 Jan;17(1):17-20. doi: 10. ...
- ... on PubMed Mehta R, Shapiro AD. Plasminogen deficiency. Haemophilia. 2008 Nov;14(6):1261-8. doi: 10. ...
- ... America with mutations in the factor 7 gene. Haemophilia. 2009 Jan;15(1):267-80. doi: 10. ...
- ... MM, Moll S. Inherited antithrombin deficiency: a review. Haemophilia. 2008 Nov;14(6):1229-39. doi: 10. ...
- ... Goldenberg NA, Manco-Johnson MJ. Protein C deficiency. Haemophilia. 2008 Nov;14(6):1214-21. doi: 10. ...
- ... Shapiro AD. Plasminogen activator inhibitor type 1 deficiency. Haemophilia. 2008 Nov;14(6):1255-60. doi: 10. ...
- ... Meer J. Protein S deficiency: a clinical perspective. Haemophilia. 2008 Nov;14(6):1222-8. doi: 10. ...
- ... Gomez K, Bolton-Maggs P. Factor XI deficiency. Haemophilia. 2008 Nov;14(6):1183-9. doi: 10. ...