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Thromb Haemost 2002; 88(04): 690-691
DOI: 10.1055/s-0037-1613279
DOI: 10.1055/s-0037-1613279
Letters to the Editor
Relatively Poor Performance of Clinical Laboratories for DNA Analyses in the Detection of Two Thrombophilic Mutations – A Cause for Concern
Further Information
Publication History
Received
29 April 2002
Accepted
02 May 2002
Publication Date:
09 December 2017 (online)
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References
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- 3 Mannucci PM. Genetic hypercoagulability: prevention suggests testing family members. Blood 2001; 98: 21-2.
- 4 Green D. Genetic hypercoagulability: screening should be an informed choice. Blood 2001; 98: 20.
- 5 Preston FE, Kitchen S, Jennings I, Woods TAL. A UK National External Quality Assessment Scheme (UK Neqas) for molecular genetic testing for the diagnosis of familial thrombophilia. Thromb Haemost 1999; 82: 1556-7.