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Fabry Disease Blood Spot Biochemistry Department, RHSC
Fabry Disease: alpha-galactosidase A gene mutations, chromosome Xq22.1-q22.2, complete sequencing Whole Blood - EDTA Karlsruhe, Laboratory Prof Seelig
Factor Assays (Coagulation) Plasma Centre for Haemostasis and Thrombosis
Factor B Serum Cardiff Medical Biochemistry and Immunology
Factor V deficiency Mutation screening Whole Blood - EDTA Centre for Haemostasis and Thrombosis
Factor V Genotype Whole Blood - EDTA Stoke-on-Trent, University Hospital of North Staffordshire, Department of Clinical Biochemistry
Factor V Leiden Plasma - EDTA Centre for Haemostasis and Thrombosis
Factor V Leiden Whole Blood - EDTA Birmingham Heartlands Hospital, Haematology Department
Factor V Leiden mutation Whole Blood - EDTA Karlsruhe, Laboratory Prof Seelig
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